ANTICAVITY- sodium fluoride mouthwash 
Vi-Jon, LLC

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Anticavity Fluoride RinseMint
163.005/163AF AG

Active Ingredient

Sodium Fluoride 0.0221% (0.01% Fluoride ion)

Purpose

Anticavity

Use

aids in the prevention of dental cavities

WARNINGS

WARNINGS

Keep out of the 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 12 years of age and older  
• use twice daily after brushing your teeth with a toothpaste
• vigorously swish 10 ml (2 teaspoonfuls) of rinse between your teeth for 1 minute then spit out
• do not swallow the rinse
• do not eat or drink for 30 minutes after rinsing
• supervise children as necessary until capable of using without supervision
• children under 12 years of age: consult a dentist or doctor

Store

• store at controlled room temperature 20⁰ - 25⁰C (68⁰ - 77⁰F)
• cold weather may temporarily cloud this product

Inactive ingredients

water, alcohol (21.6 %v/v), sorbitol, poloxamer 407, eucalyptol, flavor, methyl salicylate, menthol, phosphoric acid, sodium saccharin, thymol, disodium phosphate, sucralose, red 40, blue 1

This product is not manufactured or distributed by Johnson + Johnson Healthcare Products,
distributor of Listerine Total Care Fresh Mint Anticavity Mouthwash.

Adverse reactions

Distributed by:

Vi-Jon, LLC

One Swan Drive

Smyrna, TN 37167

principal display panel

Sealed With Printed Neckband For Your Protection

Swan

ANTICAVITY

Fluoride

Rinse

SODIUM FLUORIDE AND ACIDULATED PHOSPHATE TOPICAL SOLUTION

eucalyptus mint

  • Restores Enamel
  • Freshens Breath
  • Helps Prevent Cavities
  • Helps Strengthen Teeth
  • Helps Kill Germs That Cause Bad Breath

Compare to the active ingredient of Listerine Total Care Fresh Mint Anticavity Mouthwash

IMPORTANT: READ DIRECTIONS FOR PROPER USE

1 LITER (33.8 FL OZ)

image description

ANTICAVITY 
sodium fluoride mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0869-0163
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
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
SORBITOL (UNII: 506T60A25R)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
EUCALYPTOL (UNII: RV6J6604TK)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
MENTHOL (UNII: L7T10EIP3A)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
SACCHARIN (UNII: FST467XS7D)  
THYMOL (UNII: 3J50XA376E)  
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0869-0163-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/13/200603/26/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02105/13/200603/26/2024
Labeler - Vi-Jon, LLC (088520668)
Registrant - Consumer Product Partners, LLC (119091520)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091514manufacture(0869-0163)

Revised: 3/2024
 
Vi-Jon, LLC