Crest 3D White Whitening Therapy Charcoal

Crest 3D White Whitening Therapy Charcoal by

Drug Labeling and Warnings

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

Drug Details [pdf]

CREST 3D WHITE WHITENING THERAPY CHARCOAL- sodium fluoride paste, dentifrice 
The Procter & Gamble Manufacturing Company

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Crest 3D White Whitening Therapy Charcoal

Drug Facts

Active ingredient

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

Purpose

Anticavity toothpaste

Use

helps protect against cavities

Warning

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, sodium hydroxide, flavor, cellulose gum, sodium saccharin, carbomer, charcoal powder, sucralose, polysorbate 80, mica, titanium dioxide

Questions?

1-800-492-7378

DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

PDP - 68 g Carton

Crest 3D White Whitening Therapy CharcoalTRAVEL FRIENDLY SIZE

CREST

3D WHITE

FLUORIDE ANTICAVITY TOOTHPASTE

WHITENING THERAPY

CHARCOAL

DEEP CLEAN

INVIGORATING MINT

NET WT 2.4 OZ (68g)

CREST 3D WHITE WHITENING THERAPY CHARCOAL 
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 69423-792
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
MICA (UNII: V8A1AW0880)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
SORBITOL (UNII: 506T60A25R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
Product Characteristics
ColorblackScore    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 69423-792-241 in 1 CARTON01/01/2023
168 g in 1 TUBE; Type 0: Not a Combination Product
2NDC: 69423-792-461 in 1 CARTON01/01/2023
2130 g in 1 TUBE; Type 0: Not a Combination Product
3NDC: 69423-792-013 in 1 CELLO PACK01/01/2023
31 in 1 CARTON
3130 g in 1 TUBE; Type 0: Not a Combination Product
4NDC: 69423-792-022 in 1 CELLO PACK01/01/2023
41 in 1 CARTON
4130 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02101/01/202312/01/2023
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 2/2025
Document Id: 2efd59a0-10eb-a239-e063-6394a90a8ec8
Set id: fe03eb0d-5eff-e6b2-e053-6294a90a201a
Version: 3
Effective Time: 20250225
 
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