Label: ANTICAVITY- sodium fluoride mouthwash
- NDC Code(s): 41250-435-45
- Packager: Meijer Distribution, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 3, 2023
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- Official Label (Printer Friendly)
- 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 a day 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
- Other information
- Inactive ingredients
- Questions?
- Disclaimer
- Bottle Bloating Statment
- Adverse Reactions
-
Principal display panel
NDC 41250-435-45
meijer
ANTICAVITY
Mouth Rinse
COMPARE TO LISTERINE® ANTICAVITY MOUTHRINSE ACTIVE INGREDIENT*
SODIUM FLUORIDE AND ACIDULATED PHOSPHATE TOPICAL SOLUTION
FRESH MINT
Begins working on contact
5 days to whiter teeth
Helps strenghten teeth
Kills germs that cause bad breath
IMPORTANT: READ DIRECTIONS FOR PROPER USE.
946 mL (32 FL OZ) 1 QT
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INGREDIENTS AND APPEARANCE
ANTICAVITY
sodium fluoride mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-435 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) ALCOHOL (UNII: 3K9958V90M) HYDROGEN PEROXIDE (UNII: BBX060AN9V) POLOXAMER 407 (UNII: TUF2IVW3M2) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SUCRALOSE (UNII: 96K6UQ3ZD4) MENTHOL (UNII: L7T10EIP3A) PHOSPHORIC ACID (UNII: E4GA8884NN) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-435-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/09/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 09/09/2015 Labeler - Meijer Distribution, Inc (006959555) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(41250-435) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(41250-435)