Crest 3D White by Procter & Gamble Manfuacturing Company Crest 3D White Charcoal

Crest 3D White by

Drug Labeling and Warnings

Crest 3D White by is a Otc medication manufactured, distributed, or labeled by Procter & Gamble Manfuacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CREST 3D WHITE CHARCOAL- sodium fluoride paste, dentifrice 
Procter & Gamble Manfuacturing Company

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Crest 3D White Charcoal

Drug Facts

Active ingredient

Sodium fluoride 0.243% (0.15% w/v fluoride ion)

Purpose

Anticavity toothpaste

Use

helps protect against cavities

Warnings

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

• 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

water, sorbitol, hydrated silica, disodium pyrophosphate, sodium lauryl sulfate, flavor, sodium hydroxide, cellulose gum, sodium saccharin, carbomer, charcoal powder, polysorbate 80, mica, titanium dioxide

Questions?

1-800-492-7378

DISTR. BY PROCTER & GAMBLE,

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 107 g Carton

IMPROVED FORMULA

Crest®

3D WHITE™

FLUORIDE ANTICAVITY TOOTHPASTE

NET WT 3.8 OZ (107 g)

ENAMEL SAFE WHITENING

CHARCOAL

Removes up to
90% of surface stains

STARTS WHITENING

AFTER 1 BRUSH

CREST 3D WHITE  CHARCOAL
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-892
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
WATER (UNII: 059QF0KO0R)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SORBITOL (UNII: 506T60A25R)
MICA (UNII: V8A1AW0880)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Product Characteristics
Color	black	Score
Shape		Size
Flavor	MINT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-892-76	2 in 1 CELLO PACK	04/26/2021
1		1 in 1 CARTON
1		107 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 69423-892-38	1 in 1 CARTON	04/26/2021
2		107 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 69423-892-27	1 in 1 CARTON	04/26/2021
3		76 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	04/26/2021	12/31/2024

Labeler - Procter & Gamble Manfuacturing Company (004238200)

Revised: 12/2025

Document Id: 459e341b-f27c-38a1-e063-6394a90ab25f

34390-5

Set id: ddcb7c13-5614-d014-e053-2a95a90aefcc

Version: 6

Effective Time: 20251210

 

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