Clinpro 5000

Sodium Fluoride


3m Espe Dental Products
Human Prescription Drug
NDC 48878-3140
Clinpro 5000 also known as Sodium Fluoride is a human prescription drug labeled by '3m Espe Dental Products'. National Drug Code (NDC) number for Clinpro 5000 is 48878-3140. This drug is available in dosage form of Paste, Dentifrice. The names of the active, medicinal ingredients in Clinpro 5000 drug includes Sodium Fluoride - 5 mg/g . The currest status of Clinpro 5000 drug is Active.

Drug Information:

Drug NDC: 48878-3140
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: Clinpro 5000
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: Sodium Fluoride
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: 3m Espe Dental Products
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Paste, Dentifrice
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:SODIUM FLUORIDE - 5 mg/g
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: 07 Jan, 2011
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 31 Dec, 2025
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:3M ESPE Dental Products
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:392038
1006558
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.
UNII:8ZYQ1474W7
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.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
48878-3140-41 TUBE in 1 BOX (48878-3140-4) / 113 g in 1 TUBE07 Jan, 2011N/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:

Clinpro 5000 sodium fluoride sodium fluoride fluoride ion water sorbitol silicon dioxide glycerin polyethylene glycol, unspecified sodium lauryl sulfate titanium dioxide carboxymethylcellulose sodium saccharin sodium tricalcium phosphate mint clinpro 5000 sodium fluoride sodium fluoride fluoride ion water sorbitol silicon dioxide glycerin polyethylene glycol, unspecified sodium lauryl sulfate titanium dioxide carboxymethylcellulose sodium saccharin sodium tricalcium phosphate spearmint clinpro 5000 sodium fluoride sodium fluoride fluoride ion water sorbitol silicon dioxide glycerin polyethylene glycol, unspecified sodium lauryl sulfate titanium dioxide carboxymethylcellulose sodium saccharin sodium tricalcium phosphate bubble gum

Indications and Usage:

1 indications and usage clinpro 5000 anti-cavity toothpaste is indicated for use as part of a professional program for the prevention and control of dental caries. clinpro 5000 anti-cavity toothpaste is indicated for use as part of a professional program for the prevention and control of dental caries. ( 1 )

Warnings and Cautions:

5 warnings and precautions • do not swallow. if more than a pea-sized amount of clinpro 5000 anti-cavity toothpaste is swallowed, contact a medical or dental professional or a poison control center. • keep out of reach of children under 6 years of age. • repeated ingestion of high levels of fluoride may cause dental fluorosis. for this reason, use in children with developing dentition requires special supervision to prevent swallowing. prescribing dentists and physicians should consider risk of fluorosis when prescribing for use in children less than 6 years of age. do not swallow. ( 5 ) keep out of reach of children under 6 years of age. ( 5 ) repeated ingestion of high levels of fluoride may cause dental fluorosis. ( 5 )

Dosage and Administration:

2 dosage and administration • use once daily in place of conventional toothpaste unless instructed otherwise by a physician or dentist. • apply a thin ribbon or pea-sized amount of clinpro 5000 anti-cavity toothpaste using a soft-bristled toothbrush and brush teeth for at least two minutes. • after brushing adults should expectorate. children 6 to 16 years of age should expectorate and rinse mouth thoroughly with water. • follow these instructions or use as directed by a dental professional. use once daily in place of conventional toothpaste unless instructed otherwise by a physician or dentist. ( 2 ) apply a thin ribbon or pea-sized amount of clinpro 5000 anti-cavity toothpaste using a soft-bristled toothbrush and brush teeth for at least two minutes. ( 2 ) after brushing adults should expectorate. children 6 to 16 years of age should expectorate and rinse mouth thoroughly with water. ( 2 )

Dosage Forms and Strength:

3 dosage forms and strengths white toothpaste containing 1.1% sodium fluoride white toothpaste containing 1.1% sodium fluoride ( 3 )

Contraindications:

4 contraindications do not use in children under 6 years of age unless recommended by a dentist or physician. do not use in children under 6 years of age unless recommended by a dentist or physician. ( 4 )

Adverse Reactions:

6 adverse reactions allergic reactions and other idiosyncrasies have been rarely reported. allergic reactions and other idiosyncrasies have been rarely reported. ( 6 ) to report suspected adverse reactions, contact 3m espe dental products division at 1-800-634-2249 or www.3mespe.com , or fda at 1-800-fda-1088 or www.fda.gov/medwatch

Use in Specific Population:

8 use in specific populations 8.1 pregnancy fluoride crosses the placenta in women and has been measured in cord blood, amniotic fluid, and serum of newborn children, but without a consistent correlation to maternal serum fluoride levels. 1,2 there are no data to indicate an increased susceptibility to fluorosis during pregnancy. developmental studies were conducted by the national toxicology program, with sodium fluoride administered in the drinking water to pregnant rats and rabbits. no developmental toxicity was observed, even at doses that caused maternal toxicity. the no adverse effect levels were about 29 mg/kg-day and 27 mg/kg-day for rabbits and rats, respectively. 3 there is no conclusive evidence of fluoride developmental effects in humans. 1,2 the institute of medicine established a fluoride upper limit of 10 mg/day for pregnant women. 2 prescribing physicians and dentists should consider total fluoride exposure (dental care plus food, water and other sources) when prescribi
ng the product for use in pregnant women or women who may become pregnant. 8.3 nursing mothers an extremely small proportion of fluoride in drinking water is transferred to breast milk. the institute of medicine established a fluoride upper limit of 10 mg/day for nursing women. 2 prescribing physicians and dentists should consider total fluoride exposure (dental care plus food, water and other sources) when prescribing the product for use in women who are nursing. 8.4 pediatric use the primary adverse effects of fluoride are fluorosis of dental enamel and of the skeleton; these effects occur at exposures below those associated with other adverse health effects. the population most at risk for dental fluorosis is children during the period of tooth formation, i.e. from birth to 8 years of age. for this population, the institute of medicine established fluoride upper limits of intake based on the risk of dental fluorosis. in populations with permanent dentition, skeletal fluorosis is the greatest risk from excessive fluoride. for this population the institute of medicine (iom) established fluoride upper limits based on the risk of skeletal fluorosis. 2 population iom fluoride upper limit infants 0-6 months old 0.7 mg/day infants 7-12 months old 0.9 mg/day children 1-3 years old 1.3 mg/day children 4-8 years old 2.2 mg/day children > 8 years old 10 mg/day prescribing physicians and dentists should consider total fluoride exposure (dental care plus food, water and other sources) when prescribing the product for use in children. 8.5 geriatric use no studies of clinpro 5000 anti-cavity toothpaste have been conducted to determine whether subjects aged 65 and over respond differently from younger subjects.

Use in Pregnancy:

8.1 pregnancy fluoride crosses the placenta in women and has been measured in cord blood, amniotic fluid, and serum of newborn children, but without a consistent correlation to maternal serum fluoride levels. 1,2 there are no data to indicate an increased susceptibility to fluorosis during pregnancy. developmental studies were conducted by the national toxicology program, with sodium fluoride administered in the drinking water to pregnant rats and rabbits. no developmental toxicity was observed, even at doses that caused maternal toxicity. the no adverse effect levels were about 29 mg/kg-day and 27 mg/kg-day for rabbits and rats, respectively. 3 there is no conclusive evidence of fluoride developmental effects in humans. 1,2 the institute of medicine established a fluoride upper limit of 10 mg/day for pregnant women. 2 prescribing physicians and dentists should consider total fluoride exposure (dental care plus food, water and other sources) when prescribing the product for use in preg
nant women or women who may become pregnant.

Pediatric Use:

8.4 pediatric use the primary adverse effects of fluoride are fluorosis of dental enamel and of the skeleton; these effects occur at exposures below those associated with other adverse health effects. the population most at risk for dental fluorosis is children during the period of tooth formation, i.e. from birth to 8 years of age. for this population, the institute of medicine established fluoride upper limits of intake based on the risk of dental fluorosis. in populations with permanent dentition, skeletal fluorosis is the greatest risk from excessive fluoride. for this population the institute of medicine (iom) established fluoride upper limits based on the risk of skeletal fluorosis. 2 population iom fluoride upper limit infants 0-6 months old 0.7 mg/day infants 7-12 months old 0.9 mg/day children 1-3 years old 1.3 mg/day children 4-8 years old 2.2 mg/day children > 8 years old 10 mg/day prescribing physicians and dentists should consider total fluoride exposure (dental care plus
food, water and other sources) when prescribing the product for use in children.

Geriatric Use:

8.5 geriatric use no studies of clinpro 5000 anti-cavity toothpaste have been conducted to determine whether subjects aged 65 and over respond differently from younger subjects.

Overdosage:

10 overdosage ingestion of large amounts of fluoride may result in abdominal pain, stomach upset, nausea, vomiting, and diarrhea. these symptoms may occur at overdosages of 5 mg/kg of body weight. fluoride doses of 16 mg/kg have been fatal. treatment recommendations for overdose of clinpro 5000 anti-cavity toothpaste 4 ingested fluoride dose amount for 10 kg (22 pound) child* recommended action to take less than 5 mg/kg this equals less than ½ ounce (or less than 3 teaspoons). do not induce vomiting. give 1-2 glasses of milk and observe for symptoms of stomach upset. if symptoms persist more than a few hours, seek medical attention or contact a poison control center. 5 mg/kg or more this equals about ½ ounce (about 1 tablespoon) or more. do not induce vomiting. give 1-2 glasses of milk and seek medical attention or contact a poison control center. 15 mg/kg this equals 1 ounce or ¼ of the tube. seek immediate medical attention. do not induce vomiting. give 1-2 glasses of milk. *the amount to reach the fluoride dose will be proportionately larger with older children and adults. a thin ribbon or pea-sized amount of clinpro 5000 anti-cavity toothpaste weighs approximately 0.3 g and contains approximately 1.5 mg of fluoride ion. a 4 oz. tube contains 564 mg of fluoride ion.

Description:

11 description clinpro 5000 1.1% sodium fluoride anti-cavity toothpaste is a self-applied fluoride dentifrice for the prevention of dental caries. each gram contains 5 mg of fluoride ion in a neutral ph base, consisting of water, sorbitol, hydrated silica, glycerin, polyethylene-polypropylene glycol, flavor, polyethylene glycol, sodium lauryl sulfate, titanium dioxide, carboxymethyl cellulose, sodium saccharin and tri-calcium phosphate.

Clinical Pharmacology:

12 clinical pharmacology clinpro 5000 1.1% sodium fluoride anti-cavity toothpaste aids in the prevention of tooth decay. fluoride delivered from clinpro 5000 inhibits the demineralization of sound teeth and enhances the remineralization (i.e., repair) of demineralized teeth. during tooth brushing, fluoride is taken up by teeth and dental plaque. fluoride is taken up with calcium and phosphate by demineralized teeth resulting in an improved tooth structure than contains more fluoride and less carbonate than naturally occurring tooth structure and is more resistant to acid challenge. additionally, calcium fluoride is formed on the crystal structure of teeth. as the ph of the mouth drops, fluoride is released from calcium fluoride and aids in the remineralization of teeth. fluoride taken up into plaque alters the activity of cariogenic bacteria. fluoride inhibits the process by which cariogenic bacteria metabolize carbohydrates resulting in less acid and adhesive polysaccharide production
by the bacteria.

How Supplied:

16 how supplied/storage and handling clinpro 5000 anti-cavity toothpaste is supplied as a white dentifrice paste in a 4 oz. (113 gm) plastic tube (ndc 48878-3120-4, vanilla mint flavor; ndc 48878-3130-4 spearmint flavor; ndc 48878-3140-4 bubble gum flavor). storage this product is designed to be stored and used at room temperature. do not freeze or expose to extreme heat. see outer package for expiration date. manufactured for: 3m espe dental products 2510 conway avenue st. paul, mn 55144-1000 usa revision date: 01/11/2012 rx only 3m, espe, and clinpro are trademarks of 3m or 3m deutschland gmbh. © 3m 2016. all rights reserved.

Package Label Principal Display Panel:

Principal display panel – box label 3m espe ndc 48878-3120-4 clinpro™ 5000 vanilla mint 1.1% sodium fluoride anti-cavity toothpaste innovative tri-calcium phosphate exclusively from 3m espe contents: 1 tube net wt 4oz (113g) rx only principal display panel – box label

Principal display panel – box label 3m espe ndc 48878-3130-4 clinpro™ 5000 spearmint 1.1% sodium fluoride anti-cavity toothpaste innovative tri-calcium phosphate exclusively from 3m espe contents: 1 tube net wt 4oz (113g) rx only principal display panel – box label

Principal display panel – box label 3m espe ndc 48878-3140-4 clinpro™ 5000 bubble gum 1.1% sodium fluoride anti-cavity toothpaste innovative tri-calcium phosphate exclusively from 3m espe contents: 1 tube net wt 4oz (113g) rx only principal display panel – box label


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