Label: ANTISEPTIC MOUTH RINSE- eucalyptol mouthwash
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NDC Code(s):
0363-0072-12,
0363-0072-13,
0363-0072-69,
0363-0072-77, view more0363-0072-86, 0363-0072-88
- Packager: Walgreens Co.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated July 15, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- TEP
- Active ingredients
- Purpose
- Use
- Warnings
- Do not use
- Stop use and ask a dentist if
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
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Disclaimer
Our pharmacists recommend the Walgreens brand. We invite you to compare to nation brands.
*This product is not manufactured or distributed by Johnson & Johnson, owner of the registered tradearks Listerine and Freshburst.
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com
2021 Walgreen Co.
MADE IN THE U.S.A. WITH U.S. AND FOREIGN COMPONENTS
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principal display panel
WALGREENS - PHARMACIST RECOMMENDED
Walgreens
Compare to the active ingredients in Listine Freshburts*
Mouth Rinse
ANTIGINGIVITIS/ANTIPLAQUE
Antiseptic
- Kills germs that cause bad breath, plaque & the gum disease gingivitis
ADA Accepted
American
Dental Association
- Helps reduce plaque
- Helps reduce gingivitis
33.8 FL OZ (1 L)
Mint flavor
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INGREDIENTS AND APPEARANCE
ANTISEPTIC MOUTH RINSE
eucalyptol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0072 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) SORBITOL SOLUTION (UNII: 8KW3E207O2) POLOXAMER 407 (UNII: TUF2IVW3M2) BENZOIC ACID (UNII: 8SKN0B0MIM) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM CITRATE (UNII: 1Q73Q2JULR) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Product Characteristics Color Score Shape Size Flavor MINT (Spring Mint) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0072-77 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2007 2 NDC:0363-0072-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2007 3 NDC:0363-0072-12 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2007 4 NDC:0363-0072-13 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2007 5 NDC:0363-0072-88 2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2007 6 NDC:0363-0072-69 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/30/2007 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 03/30/2007 Labeler - Walgreens Co. (008965063) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(0363-0072)