Multitrace-5

Trace Elements 5


American Regent, Inc.
Human Prescription Drug
NDC 0517-8510
Multitrace-5 also known as Trace Elements 5 is a human prescription drug labeled by 'American Regent, Inc.'. National Drug Code (NDC) number for Multitrace-5 is 0517-8510. This drug is available in dosage form of Injection, Solution. The names of the active, medicinal ingredients in Multitrace-5 drug includes Chromic Chloride - 20.5 ug/mL Cupric Sulfate - 1.57 mg/mL Manganese Sulfate - .308 mg/mL Selenious Acid - 32.7 ug/mL Zinc Sulfate Heptahydrate - 4.39 mg/mL . The currest status of Multitrace-5 drug is Active.

Drug Information:

Drug NDC: 0517-8510
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: Multitrace-5
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: Trace Elements 5
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: American Regent, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Injection, Solution
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:CHROMIC CHLORIDE - 20.5 ug/mL
CUPRIC SULFATE - 1.57 mg/mL
MANGANESE SULFATE - .308 mg/mL
SELENIOUS ACID - 32.7 ug/mL
ZINC SULFATE HEPTAHYDRATE - 4.39 mg/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:INTRAVENOUS
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: 17 Feb, 1994
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 15 Jun, 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:American Regent, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:1293736
1293739
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UPC:0305178510253
UPC stands for Universal Product Code.
UNII:KB1PCR9DMW
LRX7AJ16DT
W00LYS4T26
F6A27P4Q4R
N57JI2K7WP
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:Copper Absorption Inhibitor [EPC]
Decreased Copper Ion Absorption [PE]
Magnetic Resonance Contrast Activity [MoA]
Paramagnetic Contrast Agent [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
0517-8510-2525 VIAL, MULTI-DOSE in 1 TRAY (0517-8510-25) / 10 mL in 1 VIAL, MULTI-DOSE17 Feb, 1994N/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:

Multitrace-5 trace elements 5 zinc sulfate heptahydrate zinc cation cupric sulfate cupric cation manganese sulfate manganese cation (2+) chromic chloride chromic cation selenious acid selenious acid benzyl alcohol sulfuric acid sodium hydroxide water

Indications and Usage:

Indications and usage this formulation is indicated for use as a supplement to intravenous solutions given for tpn. administration of the solution in tpn solutions helps to maintain plasma levels of zinc, copper, manganese, selenium and chromium and to prevent depletion of endogenous stores of these trace elements and subsequent deficiency symptoms.

Warnings:

Warnings copper and manganese are eliminated via the bile. in patients with severe liver dysfunction and/or biliary tract obstruction, decreasing or omitting copper and manganese supplements entirely may be necessary. this product contains aluminum that may be toxic. aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum. research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 mcg/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity. tissue loading may occur at even lower rates of administration.

Dosage and Administration:

Dosage and administration each ml of the solution provides zinc 1 mg, copper 0.4 mg, manganese 0.1 mg, chromium 4 mcg, and selenium 20 mcg. the suggested dosage ranges for the five trace elements are: zinc : for the metabolically stable adult receiving tpn, the suggested intravenous dosage level is 2.5 to 4 mg zinc/day. an additional 2 mg zinc/day is suggested for acute catabolic states. for the stable adult with fluid loss from the small bowel, an additional 12.2 mg zinc/liter of small bowel fluid lost, or an additional 17.1 mg zinc/kg of stool or ileostomy output is recommended. frequent monitoring of zinc blood levels is suggested for patients receiving more than the usual maintenance dosage level of zinc. normal plasma levels for zinc vary from approximately 88 to 112 mcg/100 ml. for full term infants and children up to 5 years of age, 100 mcg zinc/kg/day is recommended. for premature infants (birth weight less than 1500 g) up to 3 kg in body weight, 300 mcg zinc/kg/day is suggeste
d. copper : for the metabolically stable adult receiving tpn, the suggested additive dosage level is 0.5 to 1.5 mg copper/day. for pediatric patients, the suggested additive dosage level is 20 mcg copper/kg/day. the normal plasma range for copper is approximately 80 to 160 mcg/100 ml. manganese : for the metabolically stable adult receiving tpn, the suggested additive dosage level for manganese is 0.15 mg to 0.8 mg/day. for pediatric patients, a dosage level of 2 to 10 mcg manganese/kg/day is recommended. chromium : for the metabolically stable adult receiving tpn, the suggested additive dosage level is 10 to 15 mcg chromium/day. the metabolically stable adult with intestinal fluid loss may require 20 mcg chromium/day, with frequent monitoring of blood levels as a guideline for subsequent administration. for pediatric patients, the suggested additive dosage level is 0.14 to 0.20 mcg/kg/day. selenium : for metabolically stable adults receiving tpn, the suggested additive dosage level is 20 to 40 mcg selenium/day. for pediatric patients, the suggested additive dosage level is 3 mcg/kg/day. in adults, selenium deficiency states resulting from long term tpn support, selenium as selenomethionine or selenious acid, administered intravenously at 100 mcg/day for a period of 24 and 31 days, respectively, has been reported to reverse deficiency symptoms without toxicity. the normal whole blood range for selenium is approximately 10 to 37 mcg/100 ml. periodic monitoring of plasma levels of zinc, copper, manganese, chromium and selenium is suggested as a guideline for administration. aseptic addition of multitrace ® - 5 to parenteral nutrition solutions under laminar flow hood is recommended. the trace elements present in multitrace ® - 5 are physically compatible with the electrolytes and vitamins usually present in parenteral nutrition formulations. do not directly mix ascorbic acid injection with copper or selenium containing parenteral products in the same syringe or vial, as this admixture may cause the formation of an insoluble precipitate. parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. store at 20° to 25°c (68° to 77°f); excursions permitted to 15° to 30°c (59° to 86°f) (see usp controlled room temperature).

Contraindications:

Contraindications multitrace ® - 5 should not be given undiluted by direct injection into a peripheral vein because of the potential of infusion phlebitis.

Adverse Reactions:

Adverse reactions the amounts of zinc, copper, manganese, chromium and selenium in the solution are very small and toxicity symptoms due to these trace elements at suggested dosage levels are considered unlikely to occur.

Use in Pregnancy:

Pregnancy teratogenic effects pregnancy category c: selenium at high dosage levels (15-30 mcg/egg) has been reported to have adverse embryological effects among chickens. there are however no adequate and wellcontrolled studies in pregnant women. multitrace ® - 5 should be used during pregnancy only if potential benefit justifies the potential risk to the fetus. presence of selenium in placenta and umbilical cord blood has been reported in humans.

Overdosage:

Overdosage symptoms of zinc overdosage resulting from oral ingestion of zinc sulfate in large amounts have resulted in death. symptoms included nausea, vomiting, dehydration, electrolyte imbalances, dizziness, abdominal pain, lethargy and incoordination. single intravenous doses of 1 to 2 mg zinc/kg body weight have been given to adult leukemic patients without toxic manifestations. normal plasma levels for zinc vary from approximately 88 to 112 mcg/100 ml. plasma levels sufficient to produce symptoms of toxic manifestations are not known. calcium supplements may confer a protective effect against zinc toxicity. symptoms of copper toxicity reported in literature include prostration, behavior change, diarrhea, progressive marasmus, hypotonia, photophobia and peripheral edema. d-penicillamine has been reported effective as an antidote. manganese toxicity has not been reported in patients receiving tpn. neither have reports of manganese toxicity from excessive intake in foods and/or beverages been published. symptoms of chromium toxicity include nausea, vomiting, ulcers of gastrointestinal tract, renal and hepatic damage, and abnormalities of the central nervous system culminating in convulsions and coma. trivalent chromium administered intravenously to tpn patients has been shown to be nontoxic when given at dosage levels up to 250 mcg/day for two consecutive weeks. chronic toxicity in humans resulting from exposure to selenium in industrial environments, intake of foods grown in seleniferous soils, use of selenium contaminated water, and application of cosmetics containing selenium has been reported in literature. toxicity symptoms include hair loss, weakened nails, dermatitis, dental defects, gastrointestinal disorders, nervousness, mental depression, metallic taste, vomiting, and garlic odor of breath and sweat. acute poisoning due to ingestion of large amounts of selenium compounds has resulted in death with histopathological changes including fulminating peripheral vascular collapse, internal vascular congestion, diffusely hemorrhagic, congested and edematous lungs, brick-red color gastric mucosa. the death was preceded by coma. no effective antidote to selenium poisoning in humans is known. animal studies have shown casein and linseed oil in feeds, reduced glutathione, arsenic, magnesium sulfate, and bromobenzene to afford limited protection.

Description:

Description multitrace ® - 5 (trace elements injection 5, usp) is a sterile nonpyrogenic solution containing five trace elements for use as an additive for total parenteral nutrition (tpn). each ml provides: zinc 1 mg, copper 0.4 mg, manganese 0.1 mg, chromium 4 mcg and selenium 20 mcg. each ml contains: zinc sulfate heptahydrate 4.39 mg (equivalent to 1 mg zinc); cupric sulfate pentahydrate 1.57 mg (equivalent to 0.4 mg copper); manganese sulfate monohydrate 0.308 mg (equivalent to 0.1 mg manganese); chromic chloride hexahydrate 20.5 mcg (equivalent to 4 mcg chromium); selenious acid 32.7 mcg (equivalent to 20 mcg selenium); and water for injection q.s. ph may be adjusted with sulfuric acid and/or sodium hydroxide. 0.9% benzyl alcohol added as an antimicrobial preservative.

Clinical Pharmacology:

Clinical pharmacology zinc has been identified as a cofactor for over 70 different enzymes, including alkaline phosphatase, lactic dehydrogenase and both rna and dna polymerase. zinc facilitates wound healing, helps maintain normal growth rates, normal skin hydration and senses of taste and smell. providing zinc during tpn prevents development of the following deficiency symptoms: parakeratosis, hypogeusia, anorexia, dysosmia, geophagia, hypogonadism, growth retardation and hepatosplenomegaly. at plasma levels below 20 mcg zinc/100 ml, dermatitis followed by alopecia has been reported for tpn patients. copper is essential as a cofactor for serum ceruloplasmin, an oxidase necessary for proper formation of the iron carrier protein, transferrin. copper also helps maintain normal rates of red and white blood cell formation. scorbutic type bone changes seen in infants fed exclusively with copper-poor cow's milk are believed due to decreased activity of ascorbate oxidase, a cuproenzyme. prov
iding copper during tpn prevents development of the following deficiency symptoms: leukopenia, neutropenia, anemia, depressed ceruloplasmin levels, impaired transferrin formation and secondary iron deficiency. manganese is an activator for enzymes such as polysaccharide polymerase, liver arginase, cholinesterase and pyruvate carboxylase. providing manganese during tpn prevents development of the following deficiency symptoms: nausea and vomiting, weight loss, dermatitis, and changes in growth and color of hair. chromium (trivalent) is part of glucose tolerance factor, an activator of insulin-mediated reactions. chromium helps to maintain normal glucose metabolism and peripheral nerve function. providing chromium during tpn prevents development of the following deficiency symptoms: impaired glucose tolerance, ataxia, peripheral neuropathy and a confusional state similar to mild/moderate hepatic encephalopathy. selenium is part of glutathione peroxidase which protects cell components from oxidative damage due to peroxides produced in cellular metabolism. prolonged tpn support in humans has resulted in selenium deficiency symptoms which include muscle pain and tenderness. the symptoms have been reported to respond to supplementation of tpn solutions with selenium.

How Supplied:

How supplied multitrace ® - 5 (trace elements injection 5, usp) each ml provides: zinc 1 mg, copper 0.4 mg, manganese 0.1 mg, chromium 4 mcg, selenium 20 mcg. ndc 0517-8510-25 10 ml multiple dose vial* packaged in boxes of 25 *contains 0.9% benzyl alcohol as an antimicrobial preservative. american regent, inc. shirley, ny 11967 in8510 rev. 8/18

Package Label Principal Display Panel:

Package label.principal display panel container ndc 0517-8510-25 multitrace ® -5 (trace elements injection 5, usp) 10 ml multiple dose vial for iv use after dilution rx only carton multitrace ® -5 (trace elements injection 5, usp) ndc 0517-8510-25 25 x 10 ml multiple dose vials for iv use after dilution rx only each ml provides: zinc 1 mg, copper 0.4 mg, manganese 0.1 mg, chromium 4 mcg and selenium 20 mcg. each ml contains: zinc sulfate (heptahydrate) 4.39 mg, cupric sulfate (pentahydrate) 1.57 mg, manganese sulfate (monohydrate) 0.308 mg, chromic chloride (hexahydrate) 20.5 mcg, selenious acid 32.7 mcg, benzyl alcohol 0.9% as an antimicrobial preservative, and water for injection q.s. ph may be adjusted with sulfuric acid and/or sodium hydroxide. sterile, nonpyrogenic. store at 20°-25°c (68°-77°f); excursions permitted to 15 °-30 °c (59°-86°f) (see usp controlled room temperature). directions for use: see package insert. american regent, inc. shirley, ny 11967 rev. 11/05 10 ml container label 38cdbd24-figure-01

Serialization label serialization label


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.