Label: LISTERINE SMART RINSE ANTICAVITY FLUORIDE RINSE - MINT SHIELD- sodium fluoride mouthwash
- NDC Code(s): 69968-0689-5
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
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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
- Adults and children 6 years of age and older:
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label
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INGREDIENTS AND APPEARANCE
LISTERINE SMART RINSE ANTICAVITY FLUORIDE RINSE - MINT SHIELD
sodium fluoride mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0689 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE 0.1 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) PHOSPHORIC ACID (UNII: E4GA8884NN) CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0689-5 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 01/01/2021 Labeler - Kenvue Brands LLC (118772437)