Fluoridex

Sodium Fluoride


Dent-mat Holdings, Llc.
Human Prescription Drug
NDC 59883-031
Fluoridex also known as Sodium Fluoride is a human prescription drug labeled by 'Dent-mat Holdings, Llc.'. National Drug Code (NDC) number for Fluoridex is 59883-031. This drug is available in dosage form of Paste, Dentifrice. The names of the active, medicinal ingredients in Fluoridex drug includes Potassium Nitrate - 50 mg/g Sodium Fluoride - 5 mg/g . The currest status of Fluoridex drug is Active.

Drug Information:

Drug NDC: 59883-031
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: Fluoridex
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: Dent-mat Holdings, Llc.
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:POTASSIUM NITRATE - 50 mg/g
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:DENTAL
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: 21 Dec, 2016
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 25 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:DENT-MAT HOLDINGS, LLC.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:637365
847014
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:RU45X2JN0Z
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
59883-031-041 TUBE in 1 BOX (59883-031-04) / 112 g in 1 TUBE21 Dec, 2016N/ANo
59883-031-0524 g in 1 TUBE (59883-031-05)22 Aug, 2018N/AYes
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:

Fluoridex sodium fluoride potassium nitrate nitrate ion sodium fluoride fluoride ion clean mint

Indications and Usage:

1 indications and usage fluoridex toothpaste is indicated for use as part of a professional program for the prevention and control of dental caries.

Warnings and Cautions:

5 warnings and precautions do not swallow. • keep out of reach of children under 6 years of age. if more than used for brushing is accidentally swallowed, get medical help or contact a poison control center right away. • prolonged daily ingestion may result in various degrees of dental fluorosis in children with developing dentition, especially if the water fluoridation exceeds 0.6 ppm, since younger children frequently cannot perform the brushing process without significant swallowing. • use in children under age 6 years requires special supervision to prevent repeated swallowing of toothpaste which could cause dental fluorosis. • read directions carefully before using. • keep out of reach of infants and children. • sensitive teeth may indicate a serious problem that may need prompt care by a dentist. • see your dentist if the problem persists or worsens. do not use this product longer than 4 weeks unless recommended by a dentist or physician.

Dosage and Administration:

2 dosage and administration • follow these instructions or use as instructed by a dental professional.• adults and children age 6 or older, apply a thin ribbon or pea-sized amount of fluoridex toothpaste to a toothbrush and brush thoroughly on all tooth surfaces for at least one minute. after use: • adults should expectorate. for best results, do not eat, drink, or rinse for 30 minutes. • children, age 6 to 16, should expectorate after use and rinse mouth thoroughly. • use twice daily as your normal dentifrice or as directed by your dental professional.

Dosage Forms and Strength:

3 dosage forms and strengths 3 dosage forms and strengths • daily defense mint: green toothpaste containing 1.1% sodium fluoride (mint). (3) • daily defense fruit: pink toothpaste containing 1.1% sodium fluoride (fruit). (3) • enhanced whitening mint: green toothpaste containing 1.1% sodium fluoride (mint). (3)

Contraindications:

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

Adverse Reactions:

6 adverse reactions allergic reactions and other idiosyncrasies have rarely been reported.

Use in Specific Population:

8 use in specific populations 8.1 pregnancy pregnancy category b it has been shown that fluoride crosses the placenta of rats, but only 0.01% of the amount administered is incorporated in fetal tissues. animal studies (rats, mice, rabbits) have shown that fluoride is not a teratogen. maternal exposure to 12.2 mg fluoride/kg of body weight (rats) or 13.1 mg/kg of body weight (rabbits) did not affect the litter size or fetal weight and did not increase the frequency of skeletal or visceral malformations. there are no adequate or well controlled clinical studies in pregnant women. however, epidemiological studies conducted in areas with high levels of naturally fluoridated water showed no increase in birth defects. heavy exposure to fluoride during in utero development may result in skeletal fluorosis which becomes evident in childhood. 8.3 nursing mothers it is not known if fluoride is excreted in human milk. however, many drugs are excreted in milk, and caution should be exercised when
products containing fluoride are administered to a nursing woman. reduced milk production was reported in farm-raised fox when the animals were fed a diet containing a high concentration of fluoride (98-137 mg/kg of body weight). no adverse effects on parturition, lactation, or offspring were seen in rats administered fluoride up to 5 mg/kg of body weight. 8.4 pediatric use the use of fluoridex toothpaste in children age 6-16 as a caries preventive is supported by pioneering clinical studies with 1.1% sodium fluoride gels in mouth trays in students age 11-14 years conducted by englander, et al.2-4 safety and effectiveness in pediatric patients below the age of 6 years have not been established. 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. please refer to the contraindications and warnings and precautions sections. 8.5 geriatric use subjects referenced in clinical studies of 1.1% (w/v) sodium fluoride, included 15 percent age 65 and over, with 1 percent age 75 and over. no overall differences in safety or effectiveness were observed between these subjects and younger subjects. other reported clinical experience has not identified differences in responses between the elderly and younger clients, but greater sensitivity of some older individuals cannot be ruled out. this drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in clients with impaired renal function. because elderly clients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.

Overdosage:

10 overdosage accidental ingestion of large amounts of fluoride may result in acute burning in the mouth and sore tongue. nausea, vomiting, and diarrhea may occur soon after ingestion (within 30 minutes) and are accompanied by salivation, hematemesis, and epigastric cramping abdominal pain. these symptoms may persist for 24 hours. if less than 5 mg fluoride/kg body weight (i.e., less than 2.3 mg fluoride/lb body weight) have been ingested, give calcium (e.g., milk) orally to relieve gastrointestinal symptoms and observe for a few hours. if more than 5 mg fluoride/kg body weight (i.e., more than 2.3 mg fluoride/lb body weight) have been ingested, induce vomiting, give orally soluble calcium (e.g., milk, 5% calcium gluconate or calcium lactate solution) and immediately seek medical assistance. for accidental ingestion of more than 15 mg fluoride/kg of body weight (i.e., more than 6.9 mg fluoride/lb body weight), induce vomiting and admit immediately to a hospital facility.

Description:

11 description fluoridex toothpaste is a self-applied topical fluoride dentifrice containing 1.1% (w/w) sodium fluoride for the prevention and control of dental caries. daily defense mint: each gram contains 5 mg of fluoride ion in a neutral ph base, consisting of cellulose gum, d&c yellow no. 10, fd&c blue no. 1, flavor, glycerin, mica (and) titanium dioxide, poloxamer 234, silica, sodium laurel sulfate, sodium saccharin, sorbitol, water, xylitol. daily defense fruit: each gram contains 5 mg of fluoride ion in a neutral ph base, consisting of cellulose gum, d&c red no. 33, flavor, glycerin, mica (and) titanium dioxide, poloxamer 234, silica, sodium laurel sulfate, sodium saccharin, sorbitol, water, xylitol. enhanced whitening mint: each gram contains 5 mg of fluoride ion in a neutral ph base, consisting of cellulose gum, d&c yellow no. 10, fd&c blue no. 1, flavor, glycerin, mica (and) titanium dioxide, poloxamer 234, silica, sodium laurel sulfate, sodium saccharin, sorbitol, water, xylitol.

Clinical Pharmacology:

12 clinical pharmacology a treatment dose (a thin ribbon) of fluoridex 5000 ppm sodium fluoride toothpaste contains 2.5 mg fluoride. a 4 oz. tube contains 566 mg fluoride. frequent topical applications to the teeth with preparations having a relatively high fluoride content increase tooth resistance to acid dissolution and enhance penetration of the fluoride ion into tooth enamel.

Nonclinical Toxicology:

13 nonclinical toxicology 13.1 carcinogenesis, mutagenesis, impairment of fertility in a study conducted in rodents, no carcinogenesis was found in male and female mice and female rats treated with fluoride at dose levels ranging from 4.1 to 9.1 mg/kg of body weight. equivocal evidence of carcinogenesis was reported in male rats treated with 2.5 and 4.1 mg/kg of body weight. in a second study, no cparcinogenesis was observed in rats, males or females, treated with fluoride up to 11.3 mg/kg of body weight. epidemiological data provide no credible evidence for an association between fluoride, either naturally occurring or added to drinking water, and risk of human cancer. fluoride ion is not mutagenic in standard bacterial systems. it has been shown that fluoride ion has potential to induce chromosome aberrations in cultured human and rodent cells at doses much higher than those to which humans are exposed. in vivo data are conflicting. some studies report chromosome damage in rodents, w
hile other studies using similar protocols report negative results. potential adverse reproductive effects of fluoride exposure in humans have not been adequately evaluated. adverse effects on reproduction were reported for rats, mice, fox, and cattle exposed to 100 ppm or greater concentrations of fluoride in their diet or drinking water. other studies conducted in rats demonstrated that lower concentrations of fluoride (5 mg/kg of body w eight) did not result in impaired fertility and reproductive capabilities.

How Supplied:

16 how supplied/storage and handling 4 oz. (112 g) net wt. tube • daily defense mint ndc 59883-016-04 • daily defense fruit ndc 59883-015-04 • enhanced whitening mint ndc 59883-020-04 store at controlled room temperature 15°-30° c (59°-86° f)

Spl Patient Package Insert:

Highlights of prescribing information highlights of prescribing information ____________________________ these highlights do not include all the information needed to use fluoridex toothpaste safely and effectively. see full prescribing information. fluoridex 1.1% sodium fluoride toothpaste for oral use indications and usage _______________________________________________ fluoridex toothpaste is indicated for use as part of a professional program for the prevention and control of dental caries. (1) dosage and administration _________________________________________ • apply a thin ribbon or pea-sized amount of fluoridex toothpaste to a toothbrush and brush thoroughly on all tooth surfaces for at least one minute. (2) • after use, adults should expectorate. for best results, do not eat, drink, or rinse for 30 minutes. children, age 6-16, should expectorate after use and rinse mouth thoroughly. (2) • use twice daily as your normal dentifrice or as directed by your dental pr
ofessional. (2) dosage forms and strengths ______________________________________ • daily defense mint: green toothpaste containing 1.1% sodium fluoride (mint). (3) • daily defense fruit: pink toothpaste containing 1.1% sodium fluoride (fruit). (3) • enhanced whitening mint: green toothpaste containing 1.1% sodium fluoride (mint). (3) contraindications ___________________________________________________ do not use in children under 6 years of age unless recommended by a dentist or physician. (4) warnings and precautions _________________________________________ ● do not swallow. (5) ● keep out of reach of children under 6 years of age. if more than used for brushing is accidentally swallowed, get medical help or contact a poison control center right away. (5) ● repeated ingestion of high levels of fluoride may cause dental fluorosis. (5) ● do not use this product longer than 4 weeks unless recommended by a dentist or physician. (5) adverse reactions ___________________________________________________ allergic reactions and other idiosyncrasies have rarely been reported. (6) to report suspected adverse reactions, contact denmat, at 1-800-752-2564, or fda at 1-800-fda-1088 or www.fda.gov/medwatch

Package Label Principal Display Panel:

Principal display panel ndc59883-031-04 fluoridex sensitivity relief prescription-strength anticavity toothpaste clean mint 1.1% sodium fluoride 5000 ppm 5% potassium nitrate net wt. 4 oz. (112 g) rx only sensitive_mint


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