Crest 3D White Stain Eraser Daily Stain Prevention Luxe Mint

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-04-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:53:41

Label at a glance#

ProductCrest 3D White Stain Eraser Luxe Mint
Active ingredientSODIUM FLUORIDE
Label structure9 sections

Dosage and administration

adults and children 2 yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist do not swallow to minimize swallowing use a pea-sized amount in children under 6 supervise children's brushing until good habits are established children under 2 yrs.: ask a dentist

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Sodium fluoride 0.243%

(0.15% 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 a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist
  • do not swallow
  • to minimize swallowing use a pea-sized amount in children under 6
  • supervise children's brushing until good habits are established
  • children under 2 yrs.: ask a dentist

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, hydrated silica, sorbitol, disodium
pyrophosphate, sodium lauryl sulfate, flavor, sodium hydroxide, xanthan
gum, sodium saccharin, poloxamer 407, cocamidopropyl betaine,
sucralose, polysorbate 80, mica, titanium dioxide, blue 1

Questions?

OTC - QUESTIONS SECTION

1-800-492-7378

SPL UNCLASSIFIED SECTION

DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

Crest 3DWhite Stain Eraser Luxe Mint

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Crest

3D White

NET WT 2.3 OZ (65 g)

FLUORIDE ANTICAVITY TOOTHPASTE

STAIN ERASER

LUXE MINT

DAILY STAIN PREVENTION

ENAMEL SAFE

1.5X

MORE

FREE

vs. 0.85oz

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
891775sodium fluoride 0.243 % ToothpastePSN2
891775sodium fluoride 0.00243 MG/MG ToothpasteSCD2
891775sodium fluoride 0.243 % (fluoride ion 0.13 % ) ToothpasteSY2
891775sodium fluoride 0.243 % (fluoride ion 0.14 % ) ToothpasteSY2
891775sodium fluoride 0.243 % (fluoride ion 0.15 % ) ToothpasteSY2
891775sodium fluoride 0.243 % (fluoride ion 0.16 % ) ToothpasteSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codescan.pg.com/01/00030772247945Screenshot 2026-04-14 084534.pdf.jpg
Data codeData Matrix21428639Screenshot 2026-04-14 084534.pdf.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84126-645-23Crest 3D WhiteStain Eraser Luxe Mint65 g in 1 TUBEPASTE, DENTIFRICE652
84126-645-23Crest 3D WhiteStain Eraser Luxe Mint1 in 1 CARTONPASTE, DENTIFRICE12

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84126-64584126-645-23

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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 Stain Eraser Luxe MintSODIUM FLUORIDEThe Procter & Gamble Manufacturing Company4f6beb3b-2521-bfb7-e063-6394a90ad9ea2026-04-14Exact identifier
ndc (package): 84126-645-23
ndc (product): 84126-645
ndc11 (package): 84126064523
spl id: 4f6c7be5-d18a-df45-e063-6394a90ad3d9
spl set id: 4f6beb3b-2521-bfb7-e063-6394a90ad9ea

Reported adverse events (FAERS/openFDA)#

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