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
- 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 February 3, 2023
If you are a consumer or patient 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 0.60 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 not final part348 03/30/2007 Labeler - Walgreens Co. (008965063) Registrant - Vi Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi Jon, LLC 790752542 manufacture(0363-0072) Establishment Name Address ID/FEI Business Operations Vi Jon, LLC 088520668 manufacture(0363-0072)