CREST 3D WHITE ADVANCED RADIANT MINT- sodium fluoride paste, dentifrice 
The Procter & Gamble Manufacturing Company

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Crest 3D White Advanced Radiant Mint

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

Inactive ingredients

water, sorbitol, hydrated silica, disodium
pyrophosphate, sodium lauryl sulfate, flavor, sodium hydroxide, cellulose gum,
sodium saccharin, carbomer, polysorbate 80, mica, titanium dioxide, blue 1

Questions?

1-800-492-7378

DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 24 g Tube Carton

CREST

3D WHITE

ADVANCED

RADIANT MINT

net wt 0.85 oz (24 g)

fluoride anticavity toothpaste

ENAMEL SAFE WHITENING

REMOVES 90% MORE SURFACE STAINS*

artwork

CREST 3D WHITE  ADVANCED RADIANT MINT
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-770
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
MICA (UNII: V8A1AW0880)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
Product Characteristics
ColorblueScore    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-770-851 in 1 CARTON08/01/2021
124 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:69423-770-271 in 1 CARTON08/01/2021
276 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:69423-770-403 in 1 CELLO PACK10/11/2020
31 in 1 CARTON
3107 g in 1 TUBE; Type 0: Not a Combination Product
4NDC:69423-770-561 in 1 CARTON08/01/2021
4158 g in 1 TUBE; Type 0: Not a Combination Product
5NDC:69423-770-222 in 1 CARTON08/01/2021
576 g in 1 TUBE; Type 0: Not a Combination Product
6NDC:69423-770-922 in 1 CELLO PACK10/11/2020
61 in 1 CARTON
6107 g in 1 TUBE; Type 0: Not a Combination Product
7NDC:69423-770-381 in 1 CARTON08/01/2021
7107 g in 1 TUBE; Type 0: Not a Combination Product
8NDC:69423-770-331 in 1 CARTON10/11/2020
899 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02110/11/2020
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 2/2024
Document Id: 10aab38b-cc1a-5186-e063-6294a90a5e60
Set id: f5c89efc-5fa0-2a05-e053-2a95a90a7b9c
Version: 7
Effective Time: 20240205
 
The Procter & Gamble Manufacturing Company