Kids Anticavity Post-Brush Fluoride Rinse

Manufacturer
Wal-Mart Stores, Inc. | Vi Jon
Effective date
2010-05-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:53:11

Label at a glance#

ProductKids Anticavity Post-Brush Fluoride Rinse
Active ingredientSODIUM FLUORIDE
Label structure7 sections

Storage and handling

Other information store at 20

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION


Active ingredient                                   Purpose
Sodium Flyoride 0.0221% (0.01% w/v fluoride ion)  Anticavity

INDICATIONS & USAGE SECTION

Use aids in the prevention of dental cavities

WARNINGS SECTION

Warnings

Keep out of reach of children. If more than used for rinsing is accidentally swallowed, see professional assistance or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

• adults and children 6 years of age and older:  use twice a day after brushing your teeth with a toothpaste
• remove cap
• pour 10 milliliters (10 ML mark on inside of cap); do not fill above 10 ML mark
• vigorously swish 10 milliliters 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)
• supervisor children as necessary until capable of using without supervision
•children under 6 years of age: consult with a dentist or doctor

STORAGE AND HANDLING SECTION

Other information store at 20

INACTIVE INGREDIENT SECTION

Inactive ingredients water, sorbitol solution, propylene glycol, flavors, phosphoric acid, sucralose, cetylpyridinium chloride, disodium phosphate, methylparaben, propylparaben, yellow 6, blue 1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


IMPORTANT: READ DIRECTIONS FOR PROPER USE  

Kids
Anticavity
Post-Brush
Fluoride Rinse
See Proof in Your Sink of a Cleaner Mouth

•Helps prevent cavities

•Kills germs that cause bad breath

•Alcohol free

Mint Flavor

16.9 FL OZ (500 mL)

image of principal display panelimage of principal display panel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49035-344-772020-03-09C16284748780-19d75b9d0-2bab-f424-e053-dadaa90a57ceDrug Facts
49035-344-772020-01-31C16284748780-19d75b9d0-2bab-f424-e053-dadaa90a57ceDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SODIUM FLUORIDEACTIVE INGREDIENT8ZYQ1474W72
FLUORIDE IONACTIVE MOIETYQ80VPU408O2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-34449035-344-77

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM FLUORIDE8ZYQ1474W7ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
fd7cfa8a-a03d-474e-9930-cca79dcbf9e7ef72dc2d-b27b-49b9-aeb2-fe26ffc022182020-03-09Warnings, Adverse reactionsExact identifier
spl set id: ef72dc2d-b27b-49b9-aeb2-fe26ffc02218

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.