Label: ANTICAVITY- sodium fluoride mouthwash
- NDC Code(s): 30142-163-86
- Packager: Kroger
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 13, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Purpose
- Use
- Warnings
- Keep out of reach of children.
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Directions
Adults and children 12 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
- instruct children under 12 years of age in good rinsing habits 9to 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
- Questions or Comments?
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SPL UNCLASSIFIED SECTION
DISTRIBUTED BY THE KROGER CO.
CINCINNATI, OH 45202
Quality Guarantee
www.korger.com
*Listerine is a registered trademark of Johnson & Johnson Healthcare Products, New Brunswick, NJ 08933. Johnson & Johnson Healthcare Products is not affiliated with The Kroger Co. or this product.
DSP-TN-15000
DSP-MO-34
SDS-TN-15012
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principal display panel
Compare to the active ingredient in Listerine Total Care Anticavity Mouthwash* See back label
Kroger
Eucalyptus mint
ANICAVITY MOUTH RINSE
sodium fluoride and acidulated phosphate topical solution
- helps prevent cavities
- Restores enamel
- Helps strengthen teeth
- Kills germs that cause bad breath
- Freshens breath
Sealed with printed neckband for your protection
IMPORTANT: Read directions for proper use
1L (33.8 FL OZ)
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INGREDIENTS AND APPEARANCE
ANTICAVITY
sodium fluoride mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-163 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE 0.2 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:30142-163-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/12/2005 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 09/12/2005 Labeler - Kroger (006999528) Registrant - Vi Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi Jon, LLC 790752542 manufacture(30142-163) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(30142-163)