Crest 3D White Deep Stain Remover Ultra White

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-10-28
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
daily-update
Hydrated at
2026-11-03 06:06:26

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.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72026-07-08weekly-update2026-07-17 21:44:08
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
32025-08-19legacy-cache2026-10-22 17:42:24
22025-08-14legacy-cache2026-10-22 17:43:20

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
561a9408-3973-ad00-e063-6394a90ac8302f24a9eb-7a89-30e1-e063-6394a90a032b2026-07-08Exact identifier
spl set id: 2f24a9eb-7a89-30e1-e063-6394a90a032b

Reported adverse events (FAERS/openFDA)#

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