Crest 3D White Deep Stain Remove Enamel Strength

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-04-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:53:41

Label at a glance#

ProductCrest 3D White Deep Stain Remover Enamel Strength
Active ingredientSODIUM MONOFLUOROPHOSPHATE
Label structure9 sections

Dosage and administration

adults and children 6 yrs. & older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician. • do not swallow • children under 6 yrs.: ask a dentist

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Sodium monofluorophosphate 1.14%

(0.20% w/v fluoride ion)

Purpose

OTC - PURPOSE SECTION

Anticavity toothpaste

Use

INDICATIONS & USAGE SECTION

helps protect against cavities

Warning

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children under 6 yrs. of age. If more than used for brushing is accidentally swallowed, get medical help or contact Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 6 yrs. & older: Brush teeth
    thoroughly, preferably after each meal or at least twice a day, or as directed
    by a dentist or physician.
    • do not swallow
    • children under 6 yrs.: ask a dentist

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, sorbitol, hydrated silica, sodium hexametaphosphate, disodium
pyrophosphate, sodium lauryl sulfate, carrageenan, flavor, xanthan gum, sodium saccharin,
cocamidopropyl betaine, phosphoric acid, sucralose, mica, titanium dioxide

Questions?

OTC - QUESTIONS SECTION

1-800-492-7378

SPL UNCLASSIFIED SECTION

DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

Crest 3D White Brilliance 87g tube in carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Crest

3D WHITE

FLUORIDE ANTICAVITY TOOTHPASTE

DAILY TOOTHPASTE

DEEP STAIN REMOVER

ENAMEL STRENGTH

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038995sodium monofluorophosphate 1.14 % ToothpastePSN1
1038995sodium monofluorophosphate 0.0114 MG/MG ToothpasteSCD1
1038995sodium monofluorophosphate 1.14 % (fluoride ion 0.17 % )ToothpasteSY1
1038995sodium monofluorophosphate 1.14 % (fluoride ion 0.19 % )ToothpasteSY1
1038995sodium monofluorophosphate 1.14 % ToothpasteSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codescan.pg.com/01/00030772221310Screenshot 2026-04-14 081203.pdf.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84126-644-21Crest 3D WhiteDeep Stain Remover Enamel Strength1 in 1 CARTONPASTE, DENTIFRICE11
84126-644-21Crest 3D WhiteDeep Stain Remover Enamel Strength59 g in 1 TUBEPASTE, DENTIFRICE591
84126-644-31Crest 3D WhiteDeep Stain Remover Enamel Strength1 in 1 CARTONPASTE, DENTIFRICE11
84126-644-31Crest 3D WhiteDeep Stain Remover Enamel Strength87 g in 1 TUBEPASTE, DENTIFRICE871

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84126-64484126-644-21, 84126-644-31

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

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
Crest 3D White Deep Stain Remover Enamel StrengthSODIUM MONOFLUOROPHOSPHATEThe Procter & Gamble Manufacturing Company4f6b8851-c778-8abd-e063-6294a90aef4f2026-04-14Exact identifier
ndc (package): 84126-644-31
ndc (package): 84126-644-21
ndc (product): 84126-644
ndc11 (package): 84126064431
ndc11 (package): 84126064421
spl id: 4f6b119d-9a7f-c7fa-e063-6394a90a7e17
spl set id: 4f6b8851-c778-8abd-e063-6294a90aef4f

Reported adverse events (FAERS/openFDA)#

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