Label: ANTISPETIC- eucalyptol, menthol, methyl salicylate, thymol mouthwash
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NDC Code(s):
0363-0664-13,
0363-0664-19,
0363-0664-69,
0363-0664-77, view more0363-0664-86
- Packager: Walgreens Co
- 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 March 27, 2023
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)
- Active Ingredients
- Purpose
- Use
- Warning
- 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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Adverse Reactions
Walgreens pharmacists recommended
Our pharmacists recommend the Walgreens brand. We invite you to compare to national brands.
*This product is not manufactured or distributed by Johnson & Johnson, owner of the registered trademark Listerine and Cool Mint.
Items 834041 W10100-1222-F
DISTRIBUYTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED.
walgreens.com 1-800-925-4733
(c)2022 Walgreen Co.
Meets current TSA guidelines for carry-on luggage
DSP-TN-21091 DSP-MO-20087
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Principal display panel
SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION
Walgreens
Compare to the active ingredients in Listerine Cool Mint*
Mouth Rinse
ANTIGINGIVITIS/ANTIPLAQUE
Antiseptic/Antiplaque
- Kills germs that cause bad breath, plaque & gingivitis gum disease
- Travel Sized
ADA Accepted
American Dental Association
Helps prevent and reduce plaque
Helps prevent and reduce gingivitis
3.2 FL OZ (94mL)
Mint flavor
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INGREDIENTS AND APPEARANCE
ANTISPETIC
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0664 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 (UNII: 506T60A25R) POLOXAMER 407 (UNII: TUF2IVW3M2) BENZOIC ACID (UNII: 8SKN0B0MIM) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM BENZOATE (UNII: OJ245FE5EU) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0664-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/24/1993 2 NDC:0363-0664-77 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/24/1993 3 NDC:0363-0664-69 250 mL in 1 BOTTLE, PLASTIC; Type 1: Convenience Kit of Co-Package 03/24/1993 4 NDC:0363-0664-13 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/24/1993 5 NDC:0363-0664-19 94 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/24/1993 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 03/24/1993 Labeler - Walgreens Co (008965063) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(0363-0664) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(0363-0664)