ANTICAVITY RINSE- sodium fluoride mouthwash 
H-E-B

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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Anticavity Fluoride Rinse, Bubble Gum
004.002/004AE

Active ingredient

Sodium Fluoride 0.05% (0.02% w/v fluoride ion)        

Purpose

Anticavity Rinse

Use

aids in the prevention of dental cavities

Warnings

for this product

Keep out of reach of children.

If more than used for rinsing is accidentally swallowed, seek professional assistance or contact a Poison Control Center immediately.

Directions

Other information

Inactive ingredients

benzyl alcohol, calcium disodium EDTA, cetylpyridinium chloride, disodium EDTA, disodium phosphate, flavor, poloxomer 407, polysorbate 80, propylene glycol, red 33, sodium benzoate, sodium phosphate, sodium saccharin, sorbitol, water

MADE WITH PRIDE AND CARE FOR H-E-B,

San Antonio, TX 78204

100% GUARANTEE promise

If you arn't completely 

pleased with this product, we'll be happy to replace it or refund your money.

You have our word on it. 

how2recycle.com

US ONLY

Discard Seal, Empty & Replace Cap

Principal display panel

ADA

Accepted

American

Dental

Association

Helps prevent cavities

Sealed wth printed neckband for your protection

H-E-B

BUBBLEGUM

Anticavity

Fluoride Mouthwash

Helps prevent cavities

IMPORTANT: read directions for proper use

18 FL OZ (1.13 PT) 532 mL

image description

ANTICAVITY RINSE 
sodium fluoride mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-808
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL (UNII: LKG8494WBH)  
EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)  
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM PHOSPHATE (UNII: SE337SVY37)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-808-44532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/25/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35502/25/2010
Labeler - H-E-B (007924756)
Registrant - Vi Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi Jon, LLC790752542manufacture(37808-808)
Establishment
NameAddressID/FEIBusiness Operations
Vi Jon, LLC088520668manufacture(37808-808)

Revised: 4/2023
Document Id: 301256fc-764c-48ac-a00f-34e7fe417aaf
Set id: 51ddc81b-1c90-4998-b538-6761ac113437
Version: 10
Effective Time: 20230424
 
H-E-B