Crest 3D White

Manufacturer: The Procter & Gamble Manufacturing Company
Effective date: 2026-02-03
Label type: HUMAN OTC DRUG LABEL
Version: 9
Source: full-release
Hydrated at: 2026-06-01 01:36:35

Label at a glance#

ProductCrest 3D White Brilliance Pro Ultra White

Active ingredientSODIUM MONOFLUOROPHOSPHATE

Label structure9 sections

Dosage and administration

adults and children 12 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 12 yrs.: ask a dentist

Contacts and useful links#

PhoneLabel contact1-800-492-7378

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Sodium monofluorophosphate 1.14%

(0.17% 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 12 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 12 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 12 yrs.: ask a dentist

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, calcium pyrophosphate,
hydrogen peroxide (4% w/v), sodium lauryl sulfate, flavor, polyacrylate
crosspolymer-6, cetearyl alcohol, disodium pyrophosphate, sucralose, tetrasodium
pyrophosphate

Questions?

OTC - QUESTIONS SECTION

1-800-492-7378

SPL UNCLASSIFIED SECTION

DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

Crest 3D White Ultra White 85g tube in carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Crest

3D WHITE

FLUORIDE ANTICAVITY TOOTHPASTE

BRILLIANCE

WHITER TEETH

HYDROGEN PEROXIDE 4%

ULTRA WHITE

CLINICALLY PROVEN

-PRO-

WHITENING INGREDIENTS

NET WT 3.0 OZ (85 g)

ENAMEL SAFE

artwork

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1038995	sodium monofluorophosphate 1.14 % Toothpaste	PSN	9
1038995	sodium monofluorophosphate 0.0114 MG/MG Toothpaste	SCD	9
1038995	sodium monofluorophosphate 1.14 % (fluoride ion 0.17 % )Toothpaste	SY	9
1038995	sodium monofluorophosphate 1.14 % (fluoride ion 0.19 % )Toothpaste	SY	9
1038995	sodium monofluorophosphate 1.14 % Toothpaste	SY	9

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Data code	Data Matrix	90339204		Capture.pdf.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
69423-760-30	Crest 3D WhiteBrilliance Pro Ultra White	1 in 1 CARTON	PASTE, DENTIFRICE	1	9
69423-760-30	Crest 3D WhiteBrilliance Pro Ultra White	85 g in 1 TUBE	PASTE, DENTIFRICE	85	9
69423-760-38	Crest 3D WhiteBrilliance Pro Ultra White	107 g in 1 TUBE	PASTE, DENTIFRICE	107	9
69423-760-38	Crest 3D WhiteBrilliance Pro Ultra White	1 in 1 CARTON	PASTE, DENTIFRICE	1	9

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

Crest 3D White Brilliance Pro Ultra White
Sodium monofluorophosphate
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S)
CETOSTEARYL ALCOHOL
SODIUM PYROPHOSPHATE
GLYCERIN
HYDROGEN PEROXIDE
SODIUM LAURYL SULFATE
WATER
SUCRALOSE
FLUORIDE ION
CALCIUM PYROPHOSPHATE
SODIUM ACID PYROPHOSPHATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69423-760	69423-760-30, 69423-760-38

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S)	Q7UI015FF9	IACT
CETOSTEARYL ALCOHOL	2DMT128M1S	IACT
SODIUM PYROPHOSPHATE	O352864B8Z	IACT
GLYCERIN	PDC6A3C0OX	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
WATER	059QF0KO0R	IACT
SUCRALOSE	96K6UQ3ZD4	IACT
SODIUM MONOFLUOROPHOSPHATE	C810JCZ56Q	ACTIM
CALCIUM PYROPHOSPHATE	X69NU20D19	IACT
SODIUM ACID PYROPHOSPHATE	H5WVD9LZUD	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
8	2026-01-08	monthly-update	2026-06-03 17:51:30

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Crest 3D White Brilliance Pro Ultra White	SODIUM MONOFLUOROPHOSPHATE	The Procter & Gamble Manufacturing Company	f4c02924-95ee-09d2-e053-2995a90a8121	2026-02-03		Exact identifier ndc (package): 69423-760-38 ndc (package): 69423-760-30 ndc (product): 69423-760 ndc11 (package): 69423076030 ndc11 (package): 69423076038 spl id: 49ee5903-6e3a-c329-e063-6294a90a3be4 spl set id: f4c02924-95ee-09d2-e053-2995a90a8121

Reported adverse events (FAERS/openFDA)#

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