Label: ANTICAVITY- sodium fluoride rinse
- NDC Code(s): 41250-971-86
- Packager: Meijer Distribution, Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 16, 2024
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- Official Label (Printer Friendly)
- TEP
- Active ingredient
- Purpose
- Use
- Warning
- 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 of rinse between your teeth for 1 miute 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?
- Disclaimers
- Adverse reactions section
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Principal display panel
NDC 41250-971-86
Compare to Listerine® Total Care Zero Alcohol Active Ingredient*
meijer
ANTICAVITY
Fluoride Mouth Rinse
SODIUM FLUORIDE AND ACIDULATED PHOSPHATE TOPICAL SOLUTION
FRESH MINT
ALCOHOL FREE
6 BENEFITS:
Restores enamel
Helps prevent cavities
Kills bad breath germs
StrengthenS teeth
Freshens breath
Cleans the entire mouth**
IMPORTANT: READ DIRECTIONS FOR PROPER USE.
33.8 FL OZ (1.05 QT) 1 L
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INGREDIENTS AND APPEARANCE
ANTICAVITY
sodium fluoride rinseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-971 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) SORBITOL (UNII: 506T60A25R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLOXAMER 407 (UNII: TUF2IVW3M2) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM BENZOATE (UNII: OJ245FE5EU) PHOSPHORIC ACID (UNII: E4GA8884NN) EUCALYPTOL (UNII: RV6J6604TK) METHYL SALICYLATE (UNII: LAV5U5022Y) THYMOL (UNII: 3J50XA376E) SACCHARIN SODIUM (UNII: SB8ZUX40TY) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) SUCRALOSE (UNII: 96K6UQ3ZD4) SPEARMINT OIL (UNII: C3M81465G5) PEPPERMINT OIL (UNII: AV092KU4JH) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-971-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/11/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 02/11/2013 Labeler - Meijer Distribution, Inc (006959555) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(41250-971)