Label: REACH ANTI CAVITY FLUORIDE- sodium fluoride rinse
- NDC Code(s): 66923-300-08, 66923-300-64
- Packager: Ranir LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 27, 2022
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- Active ingredient
- Purpose
- Use
- Warnings
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Directions
Adults and children 6 years of age and older:
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- use once a day after brushing your teeth with a toothpaste
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- vigorously swish 10 mL of rinse between your teeth for 1 minute and then spit out
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- do not swallow the rinse
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- do not eat of drink for 30 minutes after rinsing
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- instruct children under 12 years of age in good rinsing habits (to minimize swallowing)
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- supervise children as necessary until capable of using without supervision
Children under 6 years of age: consult a dentist or doctor
- Other information
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
REACH ANTI CAVITY FLUORIDE
sodium fluoride rinseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66923-300 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.1 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) POLOXAMER 407 (UNII: TUF2IVW3M2) SODIUM BENZOATE (UNII: OJ245FE5EU) CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) SUCRALOSE (UNII: 96K6UQ3ZD4) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Product Characteristics Color Score Shape Size Flavor MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66923-300-08 400 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/22/2021 2 NDC:66923-300-64 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/16/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 06/22/2021 Labeler - Ranir LLC (364567615)