FDA.reportPublic FDA data

Kids Crest

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2025-01-08
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 20:42:54

Label at a glance#

ProductKids Crest Strawberry Rush
Active ingredientSODIUM FLUORIDE
Label structure10 sections

Dosage and administration

Adults and children 6 years & older: Use twice a day after brushing your teeth with a toothpaste. Vigorously swish the 10 mL (2 teaspoonfuls) 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 u...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.02% (0.01% w/v fluoride ion)

Purpose

OTC - PURPOSE SECTION

Anticavity

Use

INDICATIONS & USAGE SECTION

Aids in the prevention of dental cavities

Warning

WARNINGS SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 6 years & older: Use twice a day after brushing your teeth with a toothpaste.
  • Vigorously swish the 10 mL (2 teaspoonfuls) 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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, propylene glycol, polysorbate 80, benzoic acid, flavor, sucralose, sodium benzoate, phosphoric acid, disodium phosphate, red 33

Questions?

OTC - QUESTIONS SECTION

1-800-285-9139

SPL UNCLASSIFIED SECTION

DISTR. BY PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ALCOHOL FREE

KID'S

Crest®

ANTICAVITY

FLUORIDE RINSE

STRAWBERRY RUSH™

IMPORTANT:

Read directions

for proper use.

REACHES WHERE BRUSHING MAY MISS

500 mL

(16.9 FL OZ)

583583

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
37000-896-052023-05-18C16284748780-1ba0f9c33-2ec2-a910-e053-dadaa90a0b85Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-362023-05-18C16284748780-1ba0f9c33-2ec2-a910-e053-dadaa90a0b85Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-052023-01-30C16284748780-1ba0f9c33-2ec2-a910-e053-dadaa90a0b85Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-362023-01-30C16284748780-1ba0f9c33-2ec2-a910-e053-dadaa90a0b85Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-052021-02-12C16284748780-1ba0f9c33-2ec2-a910-e053-dadaa90a0b85Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-362021-02-12C16284748780-1ba0f9c33-2ec2-a910-e053-dadaa90a0b85Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-052021-01-29C16284748780-1ba0f9c33-2ec2-a910-e053-dadaa90a0b85Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™
37000-896-362021-01-29C16284748780-1ba0f9c33-2ec2-a910-e053-dadaa90a0b85Kid's Crest® Anticavity Fluoride Rinse Strawberry Rush™

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37000-896KIDS CREST STRAWBERRY RUSH (SODIUM FLUORIDE) RINSE [THE PROCTER & GAMBLE MANUFACTURING COMPANY]6Legacy NDC20250114_60a2e223-9f48-2f3f-e053-2991aa0abf1c.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
37000-89637000-896-05, 37000-896-36

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE70WT22SF4BIACT
BENZOIC ACID8SKN0B0MIMIACT
SUCRALOSE96K6UQ3ZD4IACT
PHOSPHORIC ACIDE4GA8884NNIACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
POLYSORBATE 806OZP39ZG8HIACT
SODIUM BENZOATEOJ245FE5EUIACT
D&C RED NO. 339DBA0SBB0LIACT
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
3a11d69d-171a-2c5d-e063-6394a90ab64660a2e223-9f48-2f3f-e053-2991aa0abf1c2025-07-16WarningsExact identifier
spl set id: 60a2e223-9f48-2f3f-e053-2991aa0abf1c

Reported adverse events (FAERS/openFDA)#

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