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

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Crest®
3D White™
Whitening Therapy
Deep Clean
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

Inactive ingredients

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

Questions?

1-800-492-7378

DISTR. BY PROCTER & GAMBLE,

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 116 g Carton

Crest®

3D WHITE™

FLUORIDE ANTICAVITY TOOTHPASTE

WHITENING

THERAPY™

charcoal

DEEP CLEAN

INVIGORATING MINT

NET WT 4.1 OZ (116 g)

215

CREST 3D WHITE WHITENING THERAPY  DEEP CLEAN CHARCOAL
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-215
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
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)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
SORBITOL (UNII: 506T60A25R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
MICA (UNII: V8A1AW0880)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorPEPPERMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-215-411 in 1 CARTON01/01/2019
1116 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:37000-215-822 in 1 CELLO PACK01/01/2019
21 in 1 CARTON
2116 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:37000-215-281 in 1 CARTON01/01/202007/20/2023
379 g in 1 TUBE; Type 0: Not a Combination Product
4NDC:37000-215-851 in 1 CARTON01/01/2020
424 g in 1 TUBE; Type 0: Not a Combination Product
5NDC:37000-215-521 in 1 CARTON01/01/2020
5147 g in 1 TUBE; Type 0: Not a Combination Product
6NDC:37000-215-033 in 1 CELLO PACK01/01/201907/20/2023
61 in 1 CARTON
6147 g in 1 TUBE; Type 0: Not a Combination Product
7NDC:37000-215-044 in 1 CELLO PACK01/01/201907/20/2023
71 in 1 CARTON
7147 g in 1 TUBE; Type 0: Not a Combination Product
8NDC:37000-215-241 in 1 CARTON01/01/2020
868 g in 1 TUBE; Type 0: Not a Combination Product
9NDC:37000-215-351 in 1 CARTON01/01/2019
999 g in 1 TUBE; Type 0: Not a Combination Product
10NDC:37000-215-602 in 1 CELLO PACK01/01/2019
101 in 1 CARTON
1099 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02101/01/2019
Labeler - Procter & Gamble Manfuacturing Company (004238200)

Revised: 2/2024
Document Id: 114d9df4-d0c9-c492-e063-6394a90a8513
Set id: 812c1519-1a4b-2495-e053-2a91aa0a914a
Version: 10
Effective Time: 20240213
 
Procter & Gamble Manfuacturing Company