Label: LISTERINE GUM THERAPY GLACIER MINT- eucalyptol, menthol, methyl salicylate, thymol mouthwash
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NDC Code(s):
69968-0790-1,
69968-0790-2,
69968-0790-3,
69968-0790-5, view more69968-0790-9
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 16, 2024
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Use
- Warnings
- Directions
- Other information
- Inactive ingredients
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 1.0 L Bottle Label
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INGREDIENTS AND APPEARANCE
LISTERINE GUM THERAPY GLACIER MINT
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0790 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTOL (UNII: RV6J6604TK) (EUCALYPTOL - UNII:RV6J6604TK) EUCALYPTOL 0.92 mg in 1 mL MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 0.42 mg in 1 mL METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 0.6 mg in 1 mL THYMOL (UNII: 3J50XA376E) (THYMOL - UNII:3J50XA376E) THYMOL 0.64 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) SORBITOL (UNII: 506T60A25R) POLOXAMER 407 (UNII: TUF2IVW3M2) BENZOIC ACID (UNII: 8SKN0B0MIM) ZINC CHLORIDE (UNII: 86Q357L16B) SODIUM BENZOATE (UNII: OJ245FE5EU) SUCRALOSE (UNII: 96K6UQ3ZD4) SACCHARIN SODIUM (UNII: SB8ZUX40TY) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0790-5 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/13/2023 2 NDC:69968-0790-1 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/13/2023 3 NDC:69968-0790-9 95 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/13/2023 4 NDC:69968-0790-2 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/01/2023 5 NDC:69968-0790-3 2 in 1 TRAY 03/01/2024 5 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 02/13/2023 Labeler - Johnson & Johnson Consumer Inc. (118772437)