Label: ANTISEPTIC- eucalyptol, menthol, methyl salicylate, thymol liquid
- NDC Code(s): 79903-153-75
- Packager: WALMART INC. (see also Equate)
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 26, 2023
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- Active ingredient
- Purposes
- Uses
- Warning
- Directions
- Other information
- Inactive ingredients
- Questions or comments
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Principal display panel
Compare to Listerine® active ingredients*
Antiseptic Mouthwash
Eucalyptol (0.092%)
Menthol (0.042%)
Methyl salicylate (0.060%)
Thymol (0.064%)
Antiplaque/antigingivitis
- Kills germs that cause plaque, gingivitis, bad breath
- Help to control and prevent plaque that leads to gingivitis
Original
L (QT PT FL OZ)
*This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., distributor of Listerine®.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND BOTTLE OR UNDER CAP IS BROKEN OR MISSING.
DISTRIBUTED BY: Walmart Inc.,
Bentonville, AR 72716
- Package label
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INGREDIENTS AND APPEARANCE
ANTISEPTIC
eucalyptol, menthol, methyl salicylate, thymol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-153 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 (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 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) POLOXAMER 407 (UNII: TUF2IVW3M2) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) BENZOIC ACID (UNII: 8SKN0B0MIM) SODIUM BENZOATE (UNII: OJ245FE5EU) CARAMEL (UNII: T9D99G2B1R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-153-75 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/30/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 12/30/2022 Labeler - WALMART INC. (see also Equate) (051957769)