Label: LISTERINE STRONG TEETH ANTICAVITY FLUORIDE MINT SHIELD- sodium fluoride mouthwash
- NDC Code(s): 69968-0696-1, 69968-0696-5
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 16, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
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Directions
- Adults and children 12 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
- Supervise children as necessary until capable of using without supervision
- Children under 12 years of age: consult a dentist or doctor
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label
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INGREDIENTS AND APPEARANCE
LISTERINE STRONG TEETH ANTICAVITY FLUORIDE MINT SHIELD
sodium fluoride mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0696 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) ALCOHOL (UNII: 3K9958V90M) POLOXAMER 407 (UNII: TUF2IVW3M2) SODIUM LAURYL SULFATE (UNII: 368GB5141J) EUCALYPTOL (UNII: RV6J6604TK) METHYL SALICYLATE (UNII: LAV5U5022Y) THYMOL (UNII: 3J50XA376E) PHOSPHORIC ACID (UNII: E4GA8884NN) SUCRALOSE (UNII: 96K6UQ3ZD4) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0696-5 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/04/2021 2 NDC:69968-0696-1 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part355 01/04/2021 Labeler - Johnson & Johnson Consumer Inc. (118772437)