Label: ANTICAVITY- sodium fluoride rinse
- NDC Code(s): 0363-0171-86
- Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 1, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- OTHER SAFETY INFORMATION
- Active Ingredients
- Purpose
- Use
- Warning
- Keep out of Reach of Children
-
Directions
Adults and children 6 years of age and older:
- use twice daily after brushing your teeth with a toothpaste
- vigorously swish 10 mL of rinse between your teeth for 1 minute and then spit out
- do not swallow the rinse
- do not eat or drink for 30 minutes after rinsing
- instruct children under 12 years of age in good rinsing habits (to minimize swallowing)
- supervise children as necessary until capable of using without supervision
Children under 6 years of age: consult a dentist or doctor
- Other information
- Inactive ingredients
- Disclaimer
-
Adverse reactions section
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com (c)2021 Walgreen Co.
MADE IN U.S.A. WITH U.S. AND FOREIGN COMPONENTS
*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.
-
Principal display panel
Walgreens
Compare to Listerine Total Care Zero Anticavity Mouthwash active ingredient**
WALGREENS PHARMACIST RECOMMENDED*
Alcohol Free
Anticavity Rinse
Mouthwash
SODIUM FLUORIDE 0.02% (0.01 W/V FLUORIDE ION) / ANTICAVITY
ALCOHOL FREE SUGAR FREE
- Helps strengthen teeth to fight cavities
- Restores enamel
- Kills bad breath germs
33.8 FL OZ (1.05 QT) 1 L
FRESH MINT flavor
IMPORTANT: Read directions for proper use
-
INGREDIENTS AND APPEARANCE
ANTICAVITY
sodium fluoride rinseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0171 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.1 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLOXAMER 407 (UNII: TUF2IVW3M2) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM BENZOATE (UNII: OJ245FE5EU) PHOSPHORIC ACID (UNII: E4GA8884NN) EUCALYPTOL (UNII: RV6J6604TK) METHYL SALICYLATE (UNII: LAV5U5022Y) THYMOL (UNII: 3J50XA376E) SACCHARIN SODIUM (UNII: SB8ZUX40TY) MENTHOL (UNII: L7T10EIP3A) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) SUCRALOSE (UNII: 96K6UQ3ZD4) SPEARMINT OIL (UNII: C3M81465G5) PEPPERMINT OIL (UNII: AV092KU4JH) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0171-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 08/11/2020 Labeler - Walgreens (008965063) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(0363-0171)