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NDC 30142-0482-86 Alcohol-Free Anticavity 0.1 mg/mL Details

Alcohol-Free Anticavity 0.1 mg/mL

Alcohol-Free Anticavity is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by The Kroger Co. The primary component is SODIUM FLUORIDE.

MedlinePlus Drug Summary

Fluoride is used to prevent tooth decay. It is taken up by teeth and helps to strengthen teeth, resist acid, and block the cavity-forming action of bacteria. Fluoride usually is prescribed for children and adults whose homes have water that is not fluoridated (already has fluoride added). This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 30142-0482-86
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Fluoride

Product Information

NDC	30142-0482
Product ID	30142-482_151183d7-d5e5-4450-8ec5-809a305ae4f8
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Alcohol-Free Anticavity
Proprietary Name Suffix	n/a
Non-Proprietary Name	Sodium fluoride
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	ORAL
Active Ingredient Strength	0.1
Active Ingredient Units	mg/mL
Substance Name	SODIUM FLUORIDE
Labeler Name	The Kroger Co
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part355
Listing Certified Through	2024-12-31

Package

Package Images

NDC 30142-0482-86 (30142048286)

Pricing Information	N/A
NDC Package Code	30142-482-86
Billing NDC	30142048286
Package	1000 mL in 1 BOTTLE, PLASTIC (30142-482-86)
Marketing Start Date	2014-05-07
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 5459eeee-adf0-4afe-b190-62d4fa113806 Details

Active ingredient

Sodium fluoride 0.02%

(0.01% w/v fluoride ion)

Purpose

Anticavity

use

aids in the prevention of dental cavities

Warning

For this product

Keep out of reach of children

If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

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
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

Inactive ingredients

water, glycerin, cetylpyridinium chloride, flavor, sodium saccharin, phosphoric acid, sodium benzoate, sucralose, poloxamer 407, benzoic acid, disodium phosphate, propylene glycol, red 33, green 3

Questions or comments

1-800-632-6900

SPL UNCLASSIFIED SECTION

Kroger

Vivid Mint

This rinse may cause temporary staining to the surface of teeth.

This is not harmful, and adequate burshing may prevent it occurence.

QUALITY GUARANTEE

800-632-6900 www.korger.com

DISTRIBUTED BY THE KROGER CO.

CINCINNATI, OHIO 45202

*Crest Pro-Health Advanced Anticavity Fluoride Mouthwash

is a registered trademark of The Procter & Gamble Company, Cincinnati, Ohio 45202.

The Procter & Gamble Company is not affiliated with The Kroger Co. or this product.

principal display panel

Vivid Mint

HELPS STRENGTHEN ENAMEL

ALCOHOL-FREE FLOURIDE MOUTHWASH

ANTICAVITY FLUORIDE RINSE

IMPORTANT: READ DIRECTIONS BEFORE USE

ENAMEL CARE

MULTI-ACTION WITH FLUORIDE

HELPS PREVENT CAVTIIES

PARABEN FREE

ALCOHOL FREE

SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION

33.8 FL OZ (1L)

INGREDIENTS AND APPEARANCE

ALCOHOL-FREE ANTICAVITY

sodium fluoride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:30142-482
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.1 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
water (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
PHOSPHORIC ACID (UNII: E4GA8884NN)
sodium benzoate (UNII: OJ245FE5EU)
sucralose (UNII: 96K6UQ3ZD4)
POLOXAMER 407 (UNII: TUF2IVW3M2)
BENZOIC ACID (UNII: 8SKN0B0MIM)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
propylene glycol (UNII: 6DC9Q167V3)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:30142-482-86	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/07/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part355	05/07/2014

Labeler - The Kroger Co (006999528)

Registrant - Vi-Jon, LLC (790752542)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		790752542	manufacture(30142-482)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		088520668	manufacture(30142-482)

Revised: 8/2022

Document Id: 151183d7-d5e5-4450-8ec5-809a305ae4f8

Set id: 5459eeee-adf0-4afe-b190-62d4fa113806

Version: 12

Effective Time: 20220829