ALCOHOL-FREE ANTICAVITY- sodium fluoride liquid 
Walgreen Co

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Sodium fluoride 0.0219% (o.o1% w/v fluoride ion)

Purpose

Anticavity

use

aids in the prevention of dental cavities

Warning Section

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

Adults and children 6 years of age and older:

Inactive ingredients

water, glycerin, flavor, cetylpyridinium chloride, phosphoric acid, methylparaben, sodium saccharin, poloxamer 407, propylparaben, propylene glycol, disodium phosphate, red 33, green 3

Questions

Call 1-888-593-0593

claim

This rinse may cause temporary staining to the surface of teeth.  This is not harmful, and adequate brushing may prevent its occurrence.

Disclaimer

This product is not manufactured or distributed by Procter + Gamble,  distributor of Crest Pro-Health Complete Anticavity Fluride Rinse

adverse reaction

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

walgreens.com

Made in the U.S.A with U.S. and foreign components

Principal Display Panel

SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION

Well at

Walgreens

ANTICAVITY FLUORIDE

Mouth rinse

IMPORTANT: read directins for proper use

MINT

Compare to Crest Pro-Health Complete Anticavity Fluoride Rinse active ingredient

33.8 FL OZ (1 L)

image description

ALCOHOL-FREE ANTICAVITY 
sodium fluoride liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0482
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.1 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
water (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0363-0482-86 1000 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part355 06/01/2013
Labeler - Walgreen Co (008965063)
Registrant - Vi-Jon (790752542)
Establishment
Name Address ID/FEI Business Operations
Vi-Jon 790752542 manufacture(0363-0482)

Revised: 7/2013
Document Id: 452b8485-2bd8-42dc-97e1-e8b4e7f9b348
Set id: 318d0551-568c-4bca-861a-201eb193b9fc
Version: 1
Effective Time: 20130715
 
Walgreen Co