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Important Safety Information
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Details
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Product Ingredients
Active Ingredient: Sodium fluoride 1.1% (w/v)
Inactive Ingredient: Purified water, sorbitol solution 70%, hydroxyethylcellulose, pluronic F-127, flavor, sodium saccharin, methyl paraben, titanium dioxide, propylparaben, certified dyes (FD&C Red #40 In Bing Cherry and Very Berry flavors, FD&C Blue #1 in Fresh Mint flavor)
Clinical Pharmacology
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.
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Characteristics
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Study Results
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Product Resources
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Indications and Usage
A dental caries preventive, for once daily self-applied topical use. PreviDent® Brush-On Gel in a squeeze-tube is easily applied onto a toothbrush as well as a mouthpiece tray. This prescription dental gel should be used once daily following use of a regular toothpaste unless otherwise instructed by your dental professional. May be used in areas where drinking water is fluoridated since topical fluoride cannot produce fluorosis. (See WARNINGS for exception.)
Contraindications
Do not use in pediatric patients under age 6 years unless recommended by a dentist or physician.
Warnings
Prolonged daily ingestion may result in various degrees of dental fluorosis in pediatric patients under age 6 years, especially if the water fluoridation exceeds 0.6 ppm. Use in pediatric patients under age 6 years requires special supervision to prevent repeated swallowing of gel. Read directions carefully before using. Keep out of reach of infants and children.
Precautions
General: Not for systemic treatment. DO NOT SWALLOW.
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 carcinogenesis 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, while other studies using similar protocols report negative results.
Potential adverse reproductive effects of fluoride exposure in humans has 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 weight) did not result in impaired fertility and reproductive capabilities.
Pregnancy: It has been shown that fluoride crosses the placenta of rats, but only 0.01% of the amount administered is incorporated in fetal tissue. 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 and well-controlled 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.
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.
Pediatric Use: The use of PreviDent Brush-On Gel in pediatric age groups 6 to 16 years as a caries preventive is supported by pioneering clinical studies with 1.1% sodium fluoride gels in mouth trays in students age 11 to 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. Please refer to the CONTRAINDICATIONS and WARNINGS sections.
Adverse Reactions
Allergic reactions and other idiosyncrasies have been rarely reported.
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.
A treatment dose (a thin ribbon) of PreviDent® Brush-On Gel contains 2 mg fluoride. A 0.8 oz. tube contains 104 mg fluoride. A 2 oz. tube contains 266 mg fluoride.
Dosage and Administration:
Follow these instructions unless otherwise instructed by your dental professional:
- After brushing thoroughly with toothpaste, rinse as usual. Adults and pediatric patients 6 years of age or older, apply a thin ribbon of gel to the teeth with a toothbrush or mouth trays once daily for at least one minute, preferably at bedtime.
- After use, adults expectorate gel. For best results, do not eat, drink or rinse for 30 minutes. Pediatric patients, age 6-16, expectorate gel after use and rinse mouth thoroughly.
How Supplied
2 oz. (56g) net wt. plastic tubes.
Very Berry: NDC 0126-0288-02
Fresh Mint: NDC 0126-0088-02Storage
Store at controlled room temperature, 20-25°C (68-77°F)
Sources
- PF DePaola, Cariology for the Nineties. Caries in our aging population: What are we learning? University of Rochester Press, Ed. WH Bowen and LW Tabak. 26-35 (1993).
- DePaola PF, In: Bower WH,Tabak LA, eds Cariology in the nineties: Caries in Our Aging Population, What are we Learning? University of Rochester Press:1993:26-35.
- Dreizen S, Brown LR, Daly TE, Drane JB. Prevention of xerostomia-related dental caries in irradiated cancer patients. J Dent Res. 1997;56:99-104.
- JR Mellberg, A Charig, M Deutchman, W O`Brien and A Lass, Effect of two fluoride gels on fluoride uptake and phosphorous loss during artificial caries formation, J Dent Res, 65(8): 1084-1096, August 1986
- LB Toolson and DE Smith, A 2-year longitudinal study of overdenture patients. Part 1: Incidence and control of caries on overdenture abutments. J Prosthet Dent, 40, 486-491.
Characteristics
- Arrests 91% of early root caries1
- Neutral pH
- Great taste and two different flavors
Benefits
- Proven clinically effective
- Safe for crowns and composite restorations
- Patient compliance
- Highest concentration of fluoride available for home use
- American Dental Association, Accepted Dental Therapeutics, Ed. 40, Chicago (1984): 405-407.
- Englander HR et al., "Clinical Anticaries Effect of Repeated Topical Sodium Fluoride Applications by Mouthpieces," JADA, 75 (1967): 638-644.
- Englander HR et al., "Residual Anticaries Effect of Repeated Topical Sodium Fluoride Applications by Mouthpieces," JADA, 78 (1969): 783-787.
- Englander HR et al., "Incremental Rates of Dental Caries After Repeated Topical Sodium Fluoride Applications in Children With Lifelong Consumption of Fluoridated Water," JADA, 82 (1971): 354-358.
Other Colgate Products Related to Caries
- Colgate® PreviDent® 5000 Booster Plus (Rx only)
- Colgate® PreviDent® 5000 Plus (Rx only)
- Colgate® PreviDent® Varnish (Rx only)
- Colgate® Phos-Flur® Rinse
- Colgate® PreviDent® 5000 Enamel Protect (Rx only)
- Colgate® 360°® Fresh 'N Protect™ Tween Toothbrush
- Colgate® 360°® Toothbrush
- Colgate® Gel-Kam® Preventative Treatment Gel
- Colgate® Kids Cavity Protection Toothpaste
- Colgate® PreviDent® 5000 Dry Mouth (Rx only)
- Colgate® PreviDent® 5000 Sensitive (Rx only)
- Colgate® PreviDent® Dental Rinse (Rx only)
- Colgate® Wave™ Gum Comfort Toothbrush
- Colgate® Wave™ Toothbrush
- Colgate® Wave™ ZigZag™ Toothbrush
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Characteristics and Benefits
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How to order
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Benefits
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Description
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Ingredients
Active Ingredient: Sodium fluoride 1.1% (w/v)
Inactive Ingredient: Purified water, sorbitol solution 70%, hydroxyethylcellulose, pluronic F-127, flavor, sodium saccharin, methyl paraben, titanium dioxide, propylparaben, certified dyes (FD&C Red #40 In Bing Cherry and Very Berry flavors, FD&C Blue #1 in Fresh Mint flavor)
Clinical Pharmacology
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.
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Manufacture/Distribution
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Pharmacokinetics
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Clinical Pharmacology
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Contraindications
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Warnings
Prolonged daily ingestion may result in various degrees of dental fluorosis in pediatric patients under age 6 years, especially if the water fluoridation exceeds 0.6 ppm. Use in pediatric patients under age 6 years requires special supervision to prevent repeated swallowing of gel. Read directions carefully before using. Keep out of reach of infants and children.
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Precautions
General: Not for systemic treatment. DO NOT SWALLOW.
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 carcinogenesis 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, while other studies using similar protocols report negative results.
Potential adverse reproductive effects of fluoride exposure in humans has 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 weight) did not result in impaired fertility and reproductive capabilities.
Pregnancy: It has been shown that fluoride crosses the placenta of rats, but only 0.01% of the amount administered is incorporated in fetal tissue. 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 and well-controlled 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.
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.
Pediatric Use: The use of PreviDent Brush-On Gel in pediatric age groups 6 to 16 years as a caries preventive is supported by pioneering clinical studies with 1.1% sodium fluoride gels in mouth trays in students age 11 to 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. Please refer to the CONTRAINDICATIONS and WARNINGS sections.
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Adverse Reactions
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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.
A treatment dose (a thin ribbon) of PreviDent® Brush-On Gel contains 2 mg fluoride. A 0.8 oz. tube contains 104 mg fluoride. A 2 oz. tube contains 266 mg fluoride.
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Dosage and Administration
Follow these instructions unless otherwise instructed by your dental professional:
- After brushing thoroughly with toothpaste, rinse as usual. Adults and pediatric patients 6 years of age or older, apply a thin ribbon of gel to the teeth with a toothbrush or mouth trays once daily for at least one minute, preferably at bedtime.
- After use, adults expectorate gel. For best results, do not eat, drink or rinse for 30 minutes. Pediatric patients, age 6-16, expectorate gel after use and rinse mouth thoroughly.
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How Supplied
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Storage
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Directions For Use
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Interactions
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Awards