Concept Ob

Vitamin Mineral Supplement


U.s. Pharmaceutical Corporation
Human Prescription Drug
NDC 52747-620
Concept Ob also known as Vitamin Mineral Supplement is a human prescription drug labeled by 'U.s. Pharmaceutical Corporation'. National Drug Code (NDC) number for Concept Ob is 52747-620. This drug is available in dosage form of Capsule. The names of the active, medicinal ingredients in Concept Ob drug includes Ascorbic Acid - 210 mg/1 Biotin - 300 ug/1 Calcium Pantothenate - 7 mg/1 Cupric Sulfate - 800 ug/1 Cyanocobalamin - 10 ug/1 Ferrous Fumarate - 42.5 mg/1 Folic Acid - 1 mg/1 Iron - 42.5 mg/1 Magnesium Sulfate, Unspecified Form - 6.9 mg/1 Manganese Sulfate - 1.3 mg/1 and more. The currest status of Concept Ob drug is Active.

Drug Information:

Drug NDC: 52747-620
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Concept Ob
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Prescription Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Vitamin Mineral Supplement
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: U.s. Pharmaceutical Corporation
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Capsule
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:ASCORBIC ACID - 210 mg/1
BIOTIN - 300 ug/1
CALCIUM PANTOTHENATE - 7 mg/1
CUPRIC SULFATE - 800 ug/1
CYANOCOBALAMIN - 10 ug/1
FERROUS FUMARATE - 42.5 mg/1
FOLIC ACID - 1 mg/1
IRON - 42.5 mg/1
MAGNESIUM SULFATE, UNSPECIFIED FORM - 6.9 mg/1
MANGANESE SULFATE - 1.3 mg/1
NIACIN - 20 mg/1
PYRIDOXINE HYDROCHLORIDE - 25 mg/1
RIBOFLAVIN - 5 mg/1
THIAMINE MONONITRATE - 5 mg/1
ZINC SULFATE, UNSPECIFIED FORM - 18.2 mg/1
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: UNAPPROVED DRUG OTHER
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date: 01 Jan, 2009
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 06 May, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:U.S. Pharmaceutical Corporation
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
NUI:N0000193618
M0001797
M0022794
N0000175951
N0000175594
M0014839
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:PQ6CK8PD0R
6SO6U10H04
568ET80C3D
LRX7AJ16DT
P6YC3EG204
R5L488RY0Q
935E97BOY8
E1UOL152H7
DE08037SAB
W00LYS4T26
2679MF687A
68Y4CF58BV
TLM2976OFR
8K0I04919X
89DS0H96TB
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:Vitamin C [EPC]
Vitamin B12 [EPC]
Nicotinic Acid [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class CS:Ascorbic Acid [CS]
Vitamin B 12 [CS]
Nicotinic Acids [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:Analogs/Derivatives [Chemical/Ingredient]
Ascorbic Acid [CS]
Calculi Dissolution Agent [EPC]
Copper Absorption Inhibitor [EPC]
Decreased Copper Ion Absorption [PE]
Increased Large Intestinal Motility [PE]
Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
Magnesium Ion Exchange Activity [MoA]
Magnetic Resonance Contrast Activity [MoA]
Nicotinic Acid [EPC]
Nicotinic Acids [CS]
Osmotic Activity [MoA]
Osmotic Laxative [EPC]
Paramagnetic Contrast Agent [EPC]
Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
Vitamin B 12 [CS]
Vitamin B 6 [Chemical/Ingredient]
Vitamin B12 [EPC]
Vitamin B6 Analog [EPC]
Vitamin C [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
52747-620-1010 BLISTER PACK in 1 BOX (52747-620-10) / 4 CAPSULE in 1 BLISTER PACK (52747-620-04)01 Jan, 2009N/ANo
52747-620-3030 CAPSULE in 1 BOTTLE, PLASTIC (52747-620-30)01 Jan, 2009N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Product Elements:

Concept ob vitamin mineral supplement ferrous fumarate ferrous cation iron iron ascorbic acid ascorbic acid folic acid folic acid thiamine mononitrate thiamine ion thiamine riboflavin riboflavin niacin niacin calcium pantothenate pantothenic acid pyridoxine hydrochloride pyridoxine biotin biotin cyanocobalamin cyanocobalamin cupric sulfate cupric cation magnesium sulfate, unspecified form magnesium cation manganese sulfate manganous cation zinc sulfate, unspecified form zinc cation hypromellose, unspecified magnesium stearate titanium dioxide fd&c red no. 40 fd&c blue no. 1 pearl red opaque concept;ob;us

Indications and Usage:

Indications: concept obtm is a prenatal supplement designed to improve the nutritional status for women throughout pregnancy and during the postnatal period to lactating and non-lactating mothers. concept obtm may also be used to improve the nutritional status of women before conception.

Warnings and Cautions:

Warning: accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. keep this product out of reach of children. in case of accidental overdose, call a doctor or poison control center immediately. warning: folic acid alone is improper therapy in the treatment for pernicious anemia and other megaloblastic anemias where vitamin b12 is deficient. precautions: general: folic acid in doses above 0.1 mg - 0.4 mg daily may obscure pernicious anemia, in that hematological remission can occur while neurological manifestations remain progressive.

Dosage and Administration:

Dosage and administration: adults (persons over 12 years of age), one (1) capsule daily, between meals, or as prescribed by a physician. do not exceed recommended dosage. do not administer to children under the age of 12.

Contraindications:

Contraindications: concept obtm is contraindicated in patients with known hypersensitivity to any of its ingredients; also, all iron compounds are contraindicated in patients with hemosiderosis, hemochromatosis, or hemolytic anemias. pernicious anemia is a contraindication, as folic acid may obscure its signs and symptoms.

Adverse Reactions:

Adverse reactions: folic acid: allergic sensitizations have been reported following both oral and parenteral administration of folic acid. ferrous fumarate: gastrointestinal disturbances (anorexia, nausea, diarrhea, constipation) occur occasionally, but are usually mild and may subside with continuation of therapy. although the absorption of iron is best when taken between meals, giving concept obtm after meals may control occasional g.i. disturbances. concept obtm is best absorbed when taken at bedtime.

Pediatric Use:

Pediatric use: safety and effectiveness of this product have not been established in pediatric patients.

Geriatric Use:

Geriatric use: no clinical studies have been performed in patients age 65 and over to determine whether older persons respond differently from younger persons. dosage should always begin at the low end of the dosage scale and should consider that elderly persons may have decreased hepatic, renal, or cardiac function and or concomitant diseases.

Overdosage:

Overdose: iron: signs and symptoms: iron is toxic. acute overdosage of iron may cause nausea and vomiting and, in severe cases, cardiovascular collapse and death. other symptoms include pallor and cyanosis, melena, shock, drowsiness and coma. the estimated overdose of orally ingested iron is 300-mg/kg body weight. when overdoses are ingested by children, severe reactions, including fatalities, have resulted. concept obtm should be stored beyond the reach of children to prevent against accidental iron poisoning. keep this and all other drugs out of the reach of children. treatment: for specific therapy, exchange transfusion and chelating agents should be used. for general management, perform gastric lavage with sodium bicarbonate solution or milk. administer intravenous fluids and electrolytes and use oxygen.

Description:

Description: each capsule contains: ferrous fumarate (anhydrous) .....................................130 mg (equivalent to about 42.5 mg of elemental iron) polysaccharideironcomplex .....................................92.4mg (equivalent to about 42.5 mg of elemental iron) vitamin c (from proascorb c‡)..................................... 210 mg folic acid ................................................................................... 1 mg thiamine mononitrate (b1)................................................. 5 mg riboflavin (b2).......................................................................... 5 mg niacin (b3)...............................................................................20 mg d-calcium pantothenate (b5)............................................. 7 mg pyridoxine hcl (b6) ..............................................................25 mg biotin (b7)........................................................................... 300 mcg cyanocobalamin (b12) .....................................................10 mcg copper (as copper sulfate)..........................................800 mcg magnesium (as magnesium sulfate)............................6.9 mg manganese (as manganese sulfate).............................1.3 mg zinc (as zinc sulfate) ....................................................... 18.2 mg inactive ingredients: hypromellose, silicon dioxide, magnesium stearate, carmine, and candurin silver fine. clinical pharmacology: concept obtm also supplies important prenatal vitamin minerals in a formulation that was especially designed to supplement the nutritional needs of pregnant women, before, during and after pregnancy. in concept obtm, patients receive the balanced support of 14 essential vitamins and minerals, including 1 mg of folic acid. the essential role of iron supplementation for pregnant women has long been recognized. concept obtm is unique in that it utilizes two (2) different forms of iron, i.e., ferrous fumarate and polysaccharide iron complex (as cell-contracted akaganèite), making available a total of 85 mg of elemental iron per capsule as follows: ferrous fumarate (anhydrous) 130 mg polysaccharide iron complex (pic) 92.4 mg ferrous fumarate: provides about 42.5 mg of elemental iron per dose. ferrous fumarate is an anhydrous salt of a combination of ferrous iron and fumaric acid, containing 33% of iron per weight. the acute toxicity in experimental animals is low and ferrous fumarate is well tolerated clinically. as a ferrous salt, it is more efficiently absorbed in the duodenum. ferrous fumarate contrasts very favorably with the availability of the 20% of elemental iron of ferrous sulfate, and the 13% of elemental iron of ferrous gluconate. polysaccharide iron complex: provides about 42.5 mg elemental iron, as a cell-contracted akaganèite. it is a product of ferric iron complexed to a low molecular weight polysaccharide. this polysaccharide is produced by the extensive hydrolysis of starch and is a dark brown powder that dissolves in water to form a very dark brown solution, which is virtually odorless and tasteless. the most frequent cause of anemia in pregnant women is iron deficiency. because of the continuous loss of iron due to monthly menstruation, most women enter pregnancy with less than optimal iron stores. supplementation of iron must suffice to meet the needs for maternal and fetal erythropoisis, and account for daily maternal gastrointestinal losses and obligate fetal transfer and growth. iron requirements during pregnancy usually cannot be met with the average diet. (acog technical bulletin (1993): nutrition during pregnancy. p.4. number 179-april 1993: the american college of obstetricians and gynecologists, washington, d.c. 20024-2188). concept obtm does not contain calcium, as calcium may inhibit iron absorption because of the binding or conversion of ferrous salts by calcium and other minerals. calcium salts can always be prescribed separately for women at high nutritional risk, including those who do not eat adequate amounts of dairy products. the recommendation of the national academy of sciences tenth ed. 1989 national academy press, washington, d.c., suggests the supplementation of 1200 mg of calcium for pregnant and lactating women for the prevention of calcium deficiency. folic acid is a hematopoetic vitamin and has been used extensively for the prevention of neural tube defects. the need for folic acid in pregnancy, with its increased demands of the fetus, or lactation, is not being met by normal dietary sources. concept obtm capsules contain 1 mg of folic acid. neural tube defects (ntd's) are the most common birth defects that result in infant mortality and serious disability. for women with a previous pregnancy that resulted in a child with a neural tube malformation, the use of 4 mg/d of folic acid has been reported to be effective in preventing a recurrence (mrc vitamin study research group, 1991). however, earlier studies from the united kingdom suggested that lower daily doses, for example 0.36 mg, might result in a comparable reduction of a recurrence of ntd's. since neural tube closure is complete by four weeks following conception, beginning folic acid supplementation after that time is not likely to be of any value. it should be noted that a daily 4 mg dose of folic acid did not prevent all ntd's in the mrc study. patients should be cautioned that folic acid supplementation does not preclude the need for consideration for prenatal testing for ntd's (acog committee opinion, number 120, march 1993: the american college of obstetricians and gynecologists, washington d.c. 20024-2188). the u.s. public health service has recommended that all women of childbearing age in the united states who are capable of becoming pregnant should consume 0.4 mg of folic acid per day for reducing their risk of having a pregnancy affected with spina bifida or other ntd's (center of disease control, 1992). recommendation for the use of folic acid to reduce the number of cases of spina bifida and other neural tube defects: mmwr 1992: 41(rr14): 1-7). concept obtm has been formulated without the addition of vitamins a, d, e and k. these fat-soluble vitamins can accumulate and lead to birth defects. supplementation of vitamins a, d, e and k should be based on an individual need assessment. all concepttm products include a unique patented source of iron, e.g. ferrous fumarate and polysaccharide iron complex (u.s. patent no: 11/243,043 pending). an increase in tolerability is observed with the (patented formulation) and is believed to occur as the result of distributing the total iron content in the composition among compounds that ndc 52747-620-30 concept obtm prescription prenatal postnatal vitamin mineral capsules 52747620300709 back side concept ob lc-10807 rev 07/2009 provide iron to the patient's blood stream via two different mechanisms. the ferrous salts are readily absorbed in the upper gut, by direct dissolution and absorption of the ferrous iron by the bloodstream. however, the iron available from pic is absorbed in the lower gut, via an active protein transport mechanism". the concept obtm formulation also supplies additional important prenatal vitamin and minerals, which supplement the nutritional needs of pregnant women, before, during and after pregnancy. deficiencies of these ingredients are common during pregnancy and lactation. clinical studies: because ferrous fumarate is an organic complex, it contains no free ions, either ferric or ferrous. polysaccharide iron complex is clinically non-toxic. prior studies in rats demonstrated that polysaccharide iron complex (pic), administered as a single oral dose to sprague dawley rats did not produce evidence of toxicity at a dosage level of 5000 mg iron/kg: (an acute oral toxicity study in rats with polysaccharide-iron complex. t.n.merriman, m. aikman and r.e. rush, springborn laboratories. inc. spencerville, ohio study no. 3340.1 march - april 1994). other clinical studies had demonstrated that polysaccharide iron gives a good hematopoietic response with an almost complete absence of the side effects usually associated with oral iron therapy. picinni and ricciotti suggested in 1982, that "the therapeutic effectiveness of polysaccharide iron complex when compared with iron fumarate in the treatment of iron deficiency anemia, appears to be as active as the iron fumarate and as well tolerated, however, it exerted a greater influence on the level of hemoglobin and on the number of red cells..." and that, "it has been exceptionally well tolerated by all patients" (picinni, l.-ricciotti, m. 1982. therapeutic effectiveness of an iron-polysaccharide complex in comparison with iron fumarate in the treatment of iron deficiency anemias): panminerva medica-europa medica, vol. 24, no. 3, pp. 213-220 (july - september 1982). as mentioned above, the patented source of iron used in concept obtm (ferrous fumarate and polysaccharide iron complex) provides a high level of elemental iron with a low incidence of gastric distress. conclusion: based on the results of this study, the oral combination of ferrous fumarate and polysaccharide iron complex was better tolerated and safer than the oral administration of ferrous fumarate alone. the conclusion of this research stated, that the addition of pic to ferrous fumarate surprisingly allows the same concentration of ferrous fumarate to be better tolerated than the ferrous fumarate alone. indications: concept obtm is a prenatal supplement designed to improve the nutritional status for women throughout pregnancy and during the postnatal period to lactating and non-lactating mothers. concept obtm may also be used to improve the nutritional status of women before conception. contraindications: concept obtm is contraindicated in patients with known hypersensitivity to any of its ingredients; also, all iron compounds are contraindicated in patients with hemosiderosis, hemochromatosis, or hemolytic anemias. pernicious anemia is a contraindication, as folic acid may obscure its signs and symptoms. warning: accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. keep this product out of reach of children. in case of accidental overdose, call a doctor or poison control center immediately. warning: folic acid alone is improper therapy in the treatment for pernicious anemia and other megaloblastic anemias where vitamin b12 is deficient. precautions: general: folic acid in doses above 0.1 mg - 0.4 mg daily may obscure pernicious anemia, in that hematological remission can occur while neurological manifestations remain progressive. pediatric use: safety and effectiveness of this product have not been established in pediatric patients. geriatric use: no clinical studies have been performed in patients age 65 and over to determine whether older persons respond differently from younger persons. dosage should always begin at the low end of the dosage scale and should consider that elderly persons may have decreased hepatic, renal, or cardiac function and or concomitant diseases. adverse reactions: folic acid: allergic sensitizations have been reported following both oral and parenteral administration of folic acid. ferrous fumarate: gastrointestinal disturbances (anorexia, nausea, diarrhea, constipation) occur occasionally, but are usually mild and may subside with continuation of therapy. although the absorption of iron is best when taken between meals, giving concept obtm after meals may control occasional g.i. disturbances. concept obtm is best absorbed when taken at bedtime. overdose: iron: signs and symptoms: iron is toxic. acute overdosage of iron may cause nausea and vomiting and, in severe cases, cardiovascular collapse and death. other symptoms include pallor and cyanosis, melena, shock, drowsiness and coma. the estimated overdose of orally ingested iron is 300-mg/kg body weight. when overdoses are ingested by children, severe reactions, including fatalities, have resulted. concept obtm should be stored beyond the reach of children to prevent against accidental iron poisoning. keep this and all other drugs out of the reach of children. treatment: for specific therapy, exchange transfusion and chelating agents should be used. for general management, perform gastric lavage with sodium bicarbonate solution or milk. administer intravenous fluids and electrolytes and use oxygen. dosage and administration: adults (persons over 12 years of age), one (1) capsule daily, between meals, or as prescribed by a physician. do not exceed recommended dosage. do not administer to children under the age of 12. how supplied: concept ob tm are pearl red-orange opaque vcaps ® capsules printed in white with "concept ob" on the cap and "us" logo on the body. packed in child-resistant cap and light resistant bottle of 30 capsules (52747-0620-30). the listed product number is not a national drug code. instead, us pharmaceutical corporation has assigned this product code formatted according to standard industry practice to meet the formatting requirements of pharmacy and healthcare insurance computer systems. store at room temperature 15º to 30ºc (59º to 86ºf) and dry place. these statements have not been evaluated by the food and drug administration. this product is not intended to diagnose, treat, cure or prevent any disease. vcaps ® and the vcaps ® logo are trademarks used under license.

Clinical Pharmacology:

Clinical pharmacology: concept obtm also supplies important prenatal vitamin minerals in a formulation that was especially designed to supplement the nutritional needs of pregnant women, before, during and after pregnancy. in concept obtm, patients receive the balanced support of 14 essential vitamins and minerals, including 1 mg of folic acid. the essential role of iron supplementation for pregnant women has long been recognized. concept obtm is unique in that it utilizes two (2) different forms of iron, i.e., ferrous fumarate and polysaccharide iron complex (as cell-contracted akaganèite), making available a total of 85 mg of elemental iron per capsule as follows: ferrous fumarate (anhydrous) 130 mg polysaccharide iron complex (pic) 92.4 mg ferrous fumarate: provides about 42.5 mg of elemental iron per dose. ferrous fumarate is an anhydrous salt of a combination of ferrous iron and fumaric acid, containing 33% of iron per weight. the acute toxicity in experimental animals is low
and ferrous fumarate is well tolerated clinically. as a ferrous salt, it is more efficiently absorbed in the duodenum. ferrous fumarate contrasts very favorably with the availability of the 20% of elemental iron of ferrous sulfate, and the 13% of elemental iron of ferrous gluconate. polysaccharide iron complex: provides about 42.5 mg elemental iron, as a cell-contracted akaganèite. it is a product of ferric iron complexed to a low molecular weight polysaccharide. this polysaccharide is produced by the extensive hydrolysis of starch and is a dark brown powder that dissolves in water to form a very dark brown solution, which is virtually odorless and tasteless. the most frequent cause of anemia in pregnant women is iron deficiency. because of the continuous loss of iron due to monthly menstruation, most women enter pregnancy with less than optimal iron stores. supplementation of iron must suffice to meet the needs for maternal and fetal erythropoisis, and account for daily maternal gastrointestinal losses and obligate fetal transfer and growth. iron requirements during pregnancy usually cannot be met with the average diet. (acog technical bulletin (1993): nutrition during pregnancy. p.4. number 179-april 1993: the american college of obstetricians and gynecologists, washington, d.c. 20024-2188). concept obtm does not contain calcium, as calcium may inhibit iron absorption because of the binding or conversion of ferrous salts by calcium and other minerals. calcium salts can always be prescribed separately for women at high nutritional risk, including those who do not eat adequate amounts of dairy products. the recommendation of the national academy of sciences tenth ed. 1989 national academy press, washington, d.c., suggests the supplementation of 1200 mg of calcium for pregnant and lactating women for the prevention of calcium deficiency. folic acid is a hematopoetic vitamin and has been used extensively for the prevention of neural tube defects. the need for folic acid in pregnancy, with its increased demands of the fetus, or lactation, is not being met by normal dietary sources. concept obtm capsules contain 1 mg of folic acid. neural tube defects (ntd's) are the most common birth defects that result in infant mortality and serious disability. for women with a previous pregnancy that resulted in a child with a neural tube malformation, the use of 4 mg/d of folic acid has been reported to be effective in preventing a recurrence (mrc vitamin study research group, 1991). however, earlier studies from the united kingdom suggested that lower daily doses, for example 0.36 mg, might result in a comparable reduction of a recurrence of ntd's. since neural tube closure is complete by four weeks following conception, beginning folic acid supplementation after that time is not likely to be of any value. it should be noted that a daily 4 mg dose of folic acid did not prevent all ntd's in the mrc study. patients should be cautioned that folic acid supplementation does not preclude the need for consideration for prenatal testing for ntd's (acog committee opinion, number 120, march 1993: the american college of obstetricians and gynecologists, washington d.c. 20024-2188). the u.s. public health service has recommended that all women of childbearing age in the united states who are capable of becoming pregnant should consume 0.4 mg of folic acid per day for reducing their risk of having a pregnancy affected with spina bifida or other ntd's (center of disease control, 1992). recommendation for the use of folic acid to reduce the number of cases of spina bifida and other neural tube defects: mmwr 1992: 41(rr14): 1-7). concept obtm has been formulated without the addition of vitamins a, d, e and k. these fat-soluble vitamins can accumulate and lead to birth defects. supplementation of vitamins a, d, e and k should be based on an individual need assessment. all concepttm products include a unique patented source of iron, e.g. ferrous fumarate and polysaccharide iron complex (u.s. patent no: 11/243,043 pending). an increase in tolerability is observed with the (patented formulation) and is believed to occur as the result of distributing the total iron content in the composition among compounds that ndc 52747-620-30 concept obtm prescription prenatal postnatal vitamin mineral capsules 52747620300709 back side concept ob lc-10807 rev 07/2009 provide iron to the patient's blood stream via two different mechanisms. the ferrous salts are readily absorbed in the upper gut, by direct dissolution and absorption of the ferrous iron by the bloodstream. however, the iron available from pic is absorbed in the lower gut, via an active protein transport mechanism". the concept obtm formulation also supplies additional important prenatal vitamin and minerals, which supplement the nutritional needs of pregnant women, before, during and after pregnancy. deficiencies of these ingredients are common during pregnancy and lactation.

Clinical Studies:

Clinical studies: because ferrous fumarate is an organic complex, it contains no free ions, either ferric or ferrous. polysaccharide iron complex is clinically non-toxic. prior studies in rats demonstrated that polysaccharide iron complex (pic), administered as a single oral dose to sprague dawley rats did not produce evidence of toxicity at a dosage level of 5000 mg iron/kg: (an acute oral toxicity study in rats with polysaccharide-iron complex. t.n.merriman, m. aikman and r.e. rush, springborn laboratories. inc. spencerville, ohio study no. 3340.1 march - april 1994). other clinical studies had demonstrated that polysaccharide iron gives a good hematopoietic response with an almost complete absence of the side effects usually associated with oral iron therapy. picinni and ricciotti suggested in 1982, that "the therapeutic effectiveness of polysaccharide iron complex when compared with iron fumarate in the treatment of iron deficiency anemia, appears to be as active as the iron fumara
te and as well tolerated, however, it exerted a greater influence on the level of hemoglobin and on the number of red cells..." and that, "it has been exceptionally well tolerated by all patients" (picinni, l.-ricciotti, m. 1982. therapeutic effectiveness of an iron-polysaccharide complex in comparison with iron fumarate in the treatment of iron deficiency anemias): panminerva medica-europa medica, vol. 24, no. 3, pp. 213-220 (july - september 1982). as mentioned above, the patented source of iron used in concept obtm (ferrous fumarate and polysaccharide iron complex) provides a high level of elemental iron with a low incidence of gastric distress. conclusion: based on the results of this study, the oral combination of ferrous fumarate and polysaccharide iron complex was better tolerated and safer than the oral administration of ferrous fumarate alone. the conclusion of this research stated, that the addition of pic to ferrous fumarate surprisingly allows the same concentration of ferrous fumarate to be better tolerated than the ferrous fumarate alone.

How Supplied:

How supplied: concept ob tm are pearl red-orange opaque vcaps ® capsules printed in white with "concept ob" on the cap and "us" logo on the body. packed in child-resistant cap and light resistant bottle of 30 capsules (52747-0620-30). the listed product number is not a national drug code. instead, us pharmaceutical corporation has assigned this product code formatted according to standard industry practice to meet the formatting requirements of pharmacy and healthcare insurance computer systems. store at room temperature 15º to 30ºc (59º to 86ºf) and dry place. these statements have not been evaluated by the food and drug administration. this product is not intended to diagnose, treat, cure or prevent any disease. vcaps ® and the vcaps ® logo are trademarks used under license.

Package Label Principal Display Panel:

Packaging concept ob


Comments/ Reviews:

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