Label: ANTICAVITY- sodium fluoride mouthwash
- NDC Code(s): 41163-043-86
- Packager: United Natural Foods, Inc. dba UNFI
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 8, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredent
- Purpose
- Use
- Warnings
- Keep out of reach of children.
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Directions
Adults and Children 6 years of age and older:
- use twice daily after brushing your teeth with a toothpaste
- vigorously swish 10 mL (2 teaspoonfuls) of rinse between your teeth for 1 minute then spit out
- do not swallow the rinse
- do not eat or drink for 30 minutes after rinsing
- 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
- Tamper Evident Statement
- Disclaimer
- Adverse Reaction
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Principal display panel
compare to Listerine® Total Care Anticavity Mouthwash active ingredient*
EQUALINE®
multiple benefit
anticavity mouthwash
sodium fluoride and acidulated phosphate topical solution
- helps strengthen teeth to help prevent cavities
- helps restore enamel
- kills germs that cause bad breath
IMPORTANT: read directions for proper use.
mint eucalyptus
33.8 FL OZ (1.05QT) 1L
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INGREDIENTS AND APPEARANCE
ANTICAVITY
sodium fluoride mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41163-043 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) ALCOHOL (UNII: 3K9958V90M) SORBITOL (UNII: 506T60A25R) POLOXAMER 407 (UNII: TUF2IVW3M2) EUCALYPTOL (UNII: RV6J6604TK) METHYL SALICYLATE (UNII: LAV5U5022Y) MENTHOL (UNII: L7T10EIP3A) PHOSPHORIC ACID (UNII: E4GA8884NN) SACCHARIN SODIUM (UNII: SB8ZUX40TY) THYMOL (UNII: 3J50XA376E) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) SUCRALOSE (UNII: 96K6UQ3ZD4) 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:41163-043-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/13/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 09/13/2009 Labeler - United Natural Foods, Inc. dba UNFI (943556183) Registrant - Vi Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi Jon, LLC 790752542 manufacture(41163-043) Establishment Name Address ID/FEI Business Operations Vi Jon, LLC 088520668 manufacture(41163-043)