Label: LISTERINE CLINICAL SOLUTIONS TEETH STRENGTH ALPINE MINT- sodium fluoride mouthwash
- NDC Code(s): 69968-0819-1, 69968-0819-5, 69968-0819-9
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
Adults and children 12 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
- supervise children as necessary until capable of using without supervision
Children under 12 years of age: consult a dentist or a doctor
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 1 L Bottle Label
ANTICAVITY FLUORIDE MOUTHWASH
LISTERINE®
CLINICAL
SOLUTIONS
IMPORTANT: READ DIRECTIONS FOR PROPER USE
SODIUM FLUORIDE & ACIDULATED PHOSPHATE TOPICAL SOLUTION
TEETH STRENGTH
Repairs enamel now to prevent cavities
for 3X stronger* and longer-lasting teeth
(*with brushing in a lab study)
ALPINE MINT
1L (1 Qt 1.8 Fl Oz)
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INGREDIENTS AND APPEARANCE
LISTERINE CLINICAL SOLUTIONS TEETH STRENGTH ALPINE MINT
sodium fluoride mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0819 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 ALCOHOL (UNII: 3K9958V90M) SORBITOL (UNII: 506T60A25R) POLOXAMER 407 (UNII: TUF2IVW3M2) SODIUM LAURYL SULFATE (UNII: 368GB5141J) PHOSPHORIC ACID (UNII: E4GA8884NN) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) SUCRALOSE (UNII: 96K6UQ3ZD4) SACCHARIN SODIUM (UNII: SB8ZUX40TY) WATER (UNII: 059QF0KO0R) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) EUCALYPTOL (UNII: RV6J6604TK) MENTHOL (UNII: L7T10EIP3A) METHYL SALICYLATE (UNII: LAV5U5022Y) THYMOL (UNII: 3J50XA376E) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0819-9 95 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/16/2023 2 NDC:69968-0819-5 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/16/2023 3 NDC:69968-0819-1 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/16/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 10/16/2023 Labeler - Kenvue Brands LLC (118772437)