FDA.reportPublic FDA data

Crest 3D White Deep Stain Remover Ultra White

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-07-08
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
weekly-update
Hydrated at
2026-07-17 21:44:08

Label at a glance#

ProductCrest 3D White Deep Stain Remover Ultra White
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

BRILLIANCE

FLUORIDE ANTICAVITY TOOTHPASTE

DEEP STAIN REMOVER

DAILY TOOTHPASTE

LABELLABEL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508

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
84126-61184126-611-21, 84126-611-31, 84126-611-04, 84126-611-03, 84126-611-02, 84126-611-85

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
HYDRATED SILICAY6O7T4G8P9IACT
SACCHARIN SODIUMSB8ZUX40TYIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
MICAV8A1AW0880IACT
SODIUM HEXAMETAPHOSPHATEP1BM4ZH95LIACT
XANTHAN GUMTTV12P4NEEIACT
SODIUM LAURYL SULFATE368GB5141JIACT
WATER059QF0KO0RIACT
SUCRALOSE96K6UQ3ZD4IACT
SODIUM ACID PYROPHOSPHATEH5WVD9LZUDIACT
CARRAGEENAN5C69YCD2YJIACT
PHOSPHORIC ACIDE4GA8884NNIACT
SORBITOL506T60A25RIACT
SODIUM MONOFLUOROPHOSPHATEC810JCZ56QACTIM

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62026-04-14full-release2026-06-01 01:53:39
52026-01-08monthly-update2026-06-03 17:51:58
42026-01-07full-release2026-06-01 01:31:41

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 Ultra WhiteSODIUM MONOFLUOROPHOSPHATEThe Procter & Gamble Manufacturing Company2f24a9eb-7a89-30e1-e063-6394a90a032b2026-07-08Exact identifier
ndc (package): 84126-611-31
ndc (package): 84126-611-85
ndc (package): 84126-611-04
ndc (package): 84126-611-21
ndc (package): 84126-611-02
ndc (package): 84126-611-03
ndc (product): 84126-611
ndc11 (package): 84126061102
ndc11 (package): 84126061131
ndc11 (package): 84126061121
ndc11 (package): 84126061185
ndc11 (package): 84126061104
ndc11 (package): 84126061103
spl id: 561a9408-3973-ad00-e063-6394a90ac830
spl set id: 2f24a9eb-7a89-30e1-e063-6394a90a032b

Reported adverse events (FAERS/openFDA)#

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