CREST SCOPE ADVANCED- sodium fluoride rinse 
The Procter & Gamble Manufacturing Company

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Crest ® Scope® Advanced™

Drug Facts

Active ingredient

Sodium Fluoride 0.02% (0.01% w/v fluoride ion)

Purpose

Anticavity

Use

Aids in the prevention of dental cavities

Warnings

Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

water, alcohol (15 wt%), propylene glycol, flavor, benzoic acid, poloxamer 407, cetylpyridinium chloride, sucralose, phosphoric acid, disodium phosphate, yellow 5, blue 1

Questions?

1-800-862-7442

DISTR. BY PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 1000mL Bottle Label

Crest®
ANTICAVITY FLUORIDE MOUTHWASH
scope®

ADVANCED

MULTI-ACTION FORMULA

+FLOURIDE

IMPORTANT: Read directions for proper use.
SEE BACK FOR IMPORTANT INGREDIENT INFORMATION.

1L (33.8 FL OZ)

LABELS

CREST SCOPE  ADVANCED
sodium fluoride rinse
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-208
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
ALCOHOL (UNII: 3K9958V90M)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
Product Characteristics
ColorgreenScore    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-208-05500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2019
2NDC:37000-208-101000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02101/01/2019
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 10/2023
Document Id: 0788f671-79fd-9f8e-e063-6394a90a4b8a
Set id: 81141f59-21d8-c8b0-e053-2a91aa0a4c56
Version: 4
Effective Time: 20231012
 
The Procter & Gamble Manufacturing Company