Follow these instructions unless otherwise instructed by your dental professional: 1. After brushing with toothpaste, adults and pediatric patients 6 years of age and older, apply a thin ribbon of gel to the teeth with a toothbrush for at least one minute, preferably at bedtime. 2. Adult patients, expectorate gel after use. For best results, do not eat, drink or rinse for 30 minutes. Pediatric patients, age 6-16, ...
Store at controlled room temperature, 20-25° C (68-77°F)
Self-topical neutral fluoride gel containing 1.1% sodium fluoride for use as a dental caries preventive in adults and pediatric patients.
Sodium Fluoride, 1.1% (w/w)
Glycerin, Hydrated Silica, Hydrogenated Starch Hydrolysate (HSH), Hydroxyapatite, Hydroxyethyl Cellulose, Natural Flavors (Mint only), Natural and Artificial Flavors (Citrus only), Polysorbate 20, Potassium Sorbate, Saccharin, Sodium Benzoate, Sodium Bicarbonate, Sodium Hydroxide, Sodium Lauryl Sulfate, Water, Xylitol
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 the tooth structure.
A dental caries preventive; for once daily self-applied topical use. It is well established that a 1.1% sodium fluoride is safe and extraordinarily effective as a caries preventive when applied frequently with mouthpiece applicators.1-4 CariFree CTx4 Gel 5000 brand of 1.1% sodium fluoride toothpaste 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)
Do not use in pediatric patients under age 6 years unless recommended by a dentist or physician.
Prolonged daily ingestion may result in various degrees of dental fluorosis in pediatric patients under age 6 years, especially if 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.
General: Not for systemic treatments. DO NOT SWALLOW.
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 provided no credible evidence for an association between fluoride, either naturally occurring or added to drinking water, and risk of human cancer.
Fluoride is not mutagenic in standard bacterial systems. It has been shows 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 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 tissue. Animal studies (rats, mice, rabbits) have shown that fluoride is not 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.
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. Reduce 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.
The use of CariFree CTx4 Gel 5000 in pediatric age group 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 Contraindications and Warnings sections.
Allergic reactions and other idiosyncrasies have been rarely reported.
Accidental ingestion of large amounts of fluoride may result in acute burning in the mouth and sore tongue. Nauseau, 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 (ie, less than 2.3 mg fluoride/lb body weight) have been ingested, give calcium (eg, milk) orally to relieve gastrointestinal symptoms and observe for a few hours. If more than 5 mg fluoride/kg body weight (ie, more than 2.3 mg fluoride/lb body weight) have been ingested, induce vomiting, give orally soluble calcium (eg, 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 (ie, 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 CariFree CTx4 Gel 5000 contains 2.5 mg fluoride. A 2 oz tube contains 284 mg fluoride.
Follow these instructions unless otherwise instructed by your dental professional:
1. After brushing with toothpaste, adults and pediatric patients 6 years of age and older, apply a thin ribbon of gel to the teeth with a toothbrush for at least one minute, preferably at bedtime.
2. Adult patients, expectorate gel after use. 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.
2 oz (56.699g) tube.
NDC# 61578-205-01 (Mint)
NDC# 61578-206-01 (Citrus)
Store at controlled room temperature, 20-25° C (68-77°F)
1. American Dental Association, Accepted Dental Therapeutics, Ed 40, Chicago (1984): 405-407.
2. HR Englander et al, “Clinical Anticaries Effect of Repeated Topical Sodium Fluoride Applications by Mouthpieces,” JADA, 75 (1967): 638-644.
3. HR Englander et al, “Residual Anticaries Effect of Repeated Topical Sodium Fluoride Applications by Mouthpieces,” JADA, 78 (1969): 783-787.
4. HR Englader 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.
CARIFREE®
PROFESSIONAL
Rx Only
Pro Gel 5000
1.1% Neutral Sodium Fluoride Anti-Cavity Toothpaste
Mint
2.4oz (68g)
NDC 61578-215-01
Description: Self-topical neutral fluoride gel containing 1.1% sodium fluoride for use as a dental caries preventive in adults and pediatric patients.
Indications & usage: For once daily self-applied topical use as a dental caries preventive in adults and pediatric patients 6 years and older.
Warnings: Not for systemic treatment. DO NOT SWALLOW. Read directions carefully before using. Keep out of reach of infants and children.
Dosage & administration
Follow these instructions unless otherwise instructed by your dental professional.
pH+® HAI NANO
U.S. PATENTS NO. 9,427,384 and 10,143,633
Questions or comments?
(800) 503-0625 or visit CariFree.com
CariFree and pH+ are registered trademarks of Oral BioTech.
Manufactured by Oral BioTech
Albany, Oregon 97321
CARIFREE®
PROFESSIONAL
Rx Only
Pro Gel 5000
1.1% Neutral Sodium Fluoride
Anti-Cavity Toothpaste
Mint
NET WT 2.4 OZ (68 g) NDC 61578-215-01
CariFree PRO Gel 5000 is for adults and children to aid in the prevention of dental caries. PRO Gel 5000 is a neutral 1.1% sodium fluoride gel containing xylitol and nanoparticle hydroxyapatite at an elevated pH promote remineralization.
Description Self-topical neutral fluoride gel containing 1.1% sodium fluoride for use as a dental caries preventive in adults and pediatric patients. |
Directions
|
| Precautions: DO NOT SWALLOW. As with all medications, keep out of reach of infants and children. Store at controlled room temperature 20–25 degreesC (68–77 degreesF). See package insert for further information. |
CARIFREE®
Questions or comments?
(800) 503-0625 or visit CariFree.com
Manufactured by Oral BioTech
Albany, Oregon 97321
3 61578 21501 3
Pro Gel 5000
1.1% Neutral Sodium Fluoride Anti-Cavity Toothpaste
Mint
Prevents Cavities
with 1.1% Sodium Fluoride
Low Abrasion Formula
Elevated pH
25% Xylitol
pH+®
nanoXIM Medical
CariFree and pH+ are registered trademarks of Oral BioTech.
U.S. Patents No. 9,427,384 and 10,143,633
CARIFREE®
PROFESSIONAL
Rx Only
Pro Gel 5000
1.1% Neutral Sodium Fluoride Anti-Cavity Toothpaste
Citrus
2.4oz (68g)
NDC 61578-216-01
Description: Self-topical neutral fluoride gel containing 1.1% sodium fluoride for use as a dental caries preventive in adults and pediatric patients.
Indications & usage: For once daily self-applied topical use as a dental caries preventive in adults and pediatric patients 6 years and older.
Warnings: Not for systemic treatment. DO NOT SWALLOW. Read directions carefully before using. Keep out of reach of infants and children.
Dosage & administration
Follow these instructions unless otherwise instructed by your dental professional.
pH+® HAI NANO
U.S. PATENTS NO. 9,427,384 and 10,143,633
Questions or comments?
(800) 503-0625 or visit CariFree.com
CariFree and pH+ are registered trademarks of Oral BioTech.
Manufactured by Oral BioTech
Albany, Oregon 97321
CARIFREE®
PROFESSIONAL
Rx Only
Pro Gel 5000
1.1% Neutral Sodium Fluoride
Anti-Cavity Toothpaste
Citrus
NET WT 2.4 OZ (68 g) NDC 61578-216-01
CariFree PRO Gel 5000 is for adults and children to aid in the prevention of dental caries. PRO Gel 5000 is a neutral 1.1% sodium fluoride gel containing xylitol and nanoparticle hydroxyapatite at an elevated pH promote remineralization.
Description Self-topical neutral fluoride gel containing 1.1% sodium fluoride for use as a dental caries preventive in adults and pediatric patients. |
Directions
|
| Precautions: DO NOT SWALLOW. As with all medications, keep out of reach of infants and children. Store at controlled room temperature 20–25 degreesC (68–77 degreesF). See package insert for further information. |
CARIFREE®
Questions or comments?
(800) 503-0625 or visit CariFree.com
Manufactured by Oral BioTech
Albany, Oregon 97321
3 61578 21601 3
Pro Gel 5000
1.1% Neutral Sodium Fluoride Anti-Cavity Toothpaste
Citrus
Prevents Cavities
with 1.1% Sodium Fluoride
Low Abrasion Formula
Elevated pH
25% Xylitol
pH+®
nanoXIM Medical
CariFree and pH+ are registered trademarks of Oral BioTech.
U.S. Patents No. 9,427,384 and 10,143,633
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 61578-215-01 | 2024-01-31 | C162847 | 48780-1 | 1030e365-6640-111a-e063-dadaa90a10e2 | Gel 5000 |
| 61578-216-01 | 2024-01-31 | C162847 | 48780-1 | 1030e365-6640-111a-e063-dadaa90a10e2 | Gel 5000 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61578-215-01 | PRO Gel 5000Mint | 68 g in 1 TUBE, WITH APPLICATOR | GEL, DENTIFRICE | 68 | 3 | |
| 61578-216-01 | PRO Gel 5000Citrus | 68 g in 1 TUBE, WITH APPLICATOR | GEL, DENTIFRICE | 68 | 3 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 61578-215 | 61578-215-01 |
| 61578-216 | 61578-216-01 |
Every source-derived ingredient row is available through these pages.
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| PRO Gel 5000 Mint | SODIUM FLUORIDE | DENTAL ALLIANCE HOLDINGS LLC | f127e236-5207-948b-e053-2a95a90ab740 | 2025-12-29 | Warnings, Adverse reactions | 61578-216-01 61578-215-01 61578-216 61578-215 61578021601 61578021501 424ae751-1f8e-4e67-ba2e-b368d447053e f127e236-5207-948b-e053-2a95a90ab740 |
Adverse event summaries are temporarily unavailable. Other product information remains available.