FDA.reportPublic FDA data

Anticavity Rinse

Manufacturer
Meijer, Inc. | Nice-Pak Products, LLC
Effective date
2026-02-19
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:46:40

Label at a glance#

ProductAnticavity Rinse
Active ingredientSODIUM FLUORIDE
Label structure13 sections

Dosage and administration

Adults and children 6 years of age and older: use once a day after brushing your teeth with a toothpaste 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) supervise children as necessary until capable of using with...

Storage and handling

Store at room temperature

Label contents#

Full prescribing information#

Tamper Evident Statement

SPL UNCLASSIFIED SECTION

SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium fluoride 0.05% (0.02% w/v fluoride ion)

Purpose

OTC - PURPOSE SECTION

Anticavity rinse

Use

INDICATIONS & USAGE SECTION

aids in the prevention of dental cavities

Warnings

WARNINGS SECTION

for this product

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If more than used for rinsing is accidentally swallowed, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 6 years of age and older:

  • use once a day after brushing your teeth with a toothpaste
  • 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)
  • supervise children as necessary until capable of using without supervision

Children under 6 years of age: consult a dentist or doctor

Other information

STORAGE AND HANDLING SECTION

Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzyl alcohol, calcium disodium EDTA, cetylpyridinium chloride, disodium EDTA, disodium phosphate, flavor, green 3, poloxamer 407, polysorbate 80, propylene glycol, sodium benzoate, sodium phosphate, sorbitol, sucralose, water, yellow 5

Questions?

OTC - QUESTIONS SECTION

 1-888-593-0593

Disclaimer

SPL UNCLASSIFIED SECTION

*This product is not manufactured or distributed by Chattem, Inc., distributor of Act ® Wild Watermelon Anticavity Kids Fluoride Rinse.

Adverse reactions

ADVERSE REACTIONS SECTION

DISTRIBUTED BY

MEIJER DISTRIBUTIONS, INC.

GRAND RAPIDS, MI 49544

www.meijer.com

OUR QUALITY GUARANTEE

The Meijer Family

WWW.MEIJER.COM/SATISFACTION

Discard Seal, Empty & Replace Cap

PLASTIC BOTTLE

how2recycle.info

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 79481-0201-1

meijer ®

KIDS

Anticavity

Fluoride Rinse

Compare to ACT ® ACTIVE INGREDIENT*

ALCOHOL FREE

WATERMELON FLAVOR

Helps prevent cavities

Helps strengthen teeth

Sugar free

18 FL OZ (1.12 PT) 532 mL

IMPORTANT: Read directions for proper use.

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240698sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral RinsePSN9
240698sodium fluoride 0.5 MG/ML MouthwashSCD9
240698sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral RinseSY9

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79481-0201-1Anticavity Rinse532 mL in 1 BOTTLE, PLASTICMOUTHWASH5329

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79481-020179481-0201-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZYL ALCOHOLLKG8494WBHIACT
EDETATE CALCIUM DISODIUM25IH6R4SGFIACT
CETYLPYRIDINIUM CHLORIDED9OM4SK49PIACT
EDETATE DISODIUM7FLD91C86KIACT
MEPREDNISONE DISODIUM PHOSPHATEW80C977F6OIACT
FD&C GREEN NO. 33P3ONR6O1SIACT
POLOXAMER 407TUF2IVW3M2IACT
POLYSORBATE 806OZP39ZG8HIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM BENZOATEOJ245FE5EUIACT
SODIUM PHOSPHATESE337SVY37IACT
SORBITOL506T60A25RIACT
SUCRALOSE96K6UQ3ZD4IACT
WATER059QF0KO0RIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
SODIUM FLUORIDE8ZYQ1474W7ACTIM

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
Anticavity RinseSODIUM FLUORIDEMeijer, Inc.b17f7a5d-272e-446d-803b-46a6d8e5f18f2026-02-19Warnings, Adverse reactionsExact identifier
ndc (package): 79481-0201-1
ndc (product): 79481-0201
ndc11 (package): 79481020101
spl id: 4b3247ad-5a19-94db-e063-6394a90a006f
spl set id: b17f7a5d-272e-446d-803b-46a6d8e5f18f

Reported adverse events (FAERS/openFDA)#

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