Label: ANTICAVITY RINSE- sodium fluoride mouthwash
- NDC Code(s): 41250-004-44
- Packager: Meijer Distribution, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 25, 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 once a day after brushing your teeth with a toothpaste
- vigorously swish 10 milliliters 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
- Adverse reactions
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Principal Panel Display
NDC 41250-004-44
meijer®
Kids Anticavity Fluoride Rinse
Compare to ACT® ACTIVE INGREDIENT*
ALCOHOL FREE
BUBBLEGUM FLAVOR
Helps prevent cavities
Helps strengthen teeth
Sugar free
Fresh & clean
ADA Accepted
American Dental Association
Helps prevent cavities
IMPORTANT: read directions for proper use
18 FL OZ (1.12 PT) 532 mL
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INGREDIENTS AND APPEARANCE
ANTICAVITY RINSE
sodium fluoride mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-004 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.2 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) EDETATE CALCIUM DISODIUM (UNII: 25IH6R4SGF) CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) EDETATE DISODIUM (UNII: 7FLD91C86K) MEPREDNISONE DISODIUM PHOSPHATE (UNII: W80C977F6O) POLOXAMER 407 (UNII: TUF2IVW3M2) POLYSORBATE 80 (UNII: 6OZP39ZG8H) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) D&C RED NO. 33 (UNII: 9DBA0SBB0L) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM PHOSPHATE (UNII: SE337SVY37) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SORBITOL (UNII: 506T60A25R) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-004-44 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/27/2002 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 06/27/2002 Labeler - Meijer Distribution, Inc. (006959555) Registrant - Vi Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi Jon, LLC 790752542 manufacture(41250-004) Establishment Name Address ID/FEI Business Operations Vi Jon, LLC 088520668 manufacture(41250-004)