Label: ALCOHOL-FREE ANTICAVITY- sodium fluoride liquid
- NDC Code(s): 79903-279-10
- Packager: Walmart Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 17, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Claims
- Tamper Evident Statement
- Active ingredient
- Purpose
- Use
- Warnings
- Keep out of reach of children.
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Directions
Adults and children 6 years of age and older:
- use twice daily after brushing your teeth with a toothpaste
- vigorously swish 10 mL (2 teaspoonfuls) of rinse between your teeth for 1 minute and then spit out
- do not swallow the rinse
- do not eat or drink for 30 minutes after rinsing
- instruct children under 12 years of age in good rinsing habits ( to minimize swallowing)
- supervise children as necessary until capable of using without supervision
- children under 6 years of age: consult a dentist or doctor
- Inactive ingredients
- Questions?
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Disclaimers
This rinse may cause temporary staining to the surface of teeth. This is not harmful, and adequate brushing may prevent its occurence.
*This product is not manufactured or distributed by Procter & Gamble, distributor of Crest ®Pro-Health ®Advanced Anticavity Fluoride Mouthwash.
**This product is not intended to replace brushing or flossing.
- Adverse reaction
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Principal display panel
NDC 79903-279-10
Compare to Crest ®Pro-Health ®Advanced Anticavity Fluoride Mouthwash active ingredient*
equate ™
Anticavity
Fluoride
Oral Rinse
Mint
Multi-Action with Fluoride
Strengthens enamel
Helps prevent cavities
Cleans teeth**
Kills bad breath germs
Helps keep mouth feeling clean
Freshens breath
No burn of alcohol
ALCOHOL FREE
IMPORTANT: Read directions for proper use.
33.8 FL OZ (1.05 QT) 1 L
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INGREDIENTS AND APPEARANCE
ALCOHOL-FREE ANTICAVITY
sodium fluoride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-279 Route of Administration ORAL 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) CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) CINNAMALDEHYDE (UNII: SR60A3XG0F) SACCHARIN SODIUM (UNII: SB8ZUX40TY) PHOSPHORIC ACID (UNII: E4GA8884NN) SODIUM BENZOATE (UNII: OJ245FE5EU) SUCRALOSE (UNII: 96K6UQ3ZD4) POLOXAMER 407 (UNII: TUF2IVW3M2) BENZOIC ACID (UNII: 8SKN0B0MIM) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-279-10 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/04/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 12/04/2024 Labeler - Walmart Inc. (051957769) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(79903-279)