ANTICAVITY- sodium fluoride mouthwash

Anticavity by

Drug Labeling and Warnings

Anticavity by is a Otc medication manufactured, distributed, or labeled by Your Military Exchanges, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Sodium fluoride 0.0221%

Purpose

Anticavity

Use

aids in the prevention of dental cavities

WARNINGS

Warnings

Keep out of reach of children.

If more than ued 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 afttr brushing your teeth with toothpaste
vigorously swish 10mL (2 teaspoonfuls) of rinse between
 your teeth for 1 minute and then spit out
do not swallow the rinse
supervise children as necessary until capable of using without supervision
children under 12 years of age: consult a dentist or doctor

Other Information

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

Inactive ingredients

water, sorbitol solution, alcohol (21.6%), flavors, poloxamer 407, sodium lauryl sulfate, phosphoric acid, sucralose and/or sodium saccharin, dibasic sodium phosphate, D+C red no.33, FD+C blue no.1, yellow no.6

SPL UNCLASSIFIED SECTION

Satisfaction Guaranteed or Your Money Back
Manufactured For Your Military Exchanges
By: Vi-Jon
8515 Page Avenue
St. Louis, MO 63114

principal display panel

Exchange Select

ANTICAVITY MOUTH RINSE

Sodium Fluoride and Acidulated Phosphate Topical Solution

EUCALYPTUS MINT

*Compare to the active ingredient in Listerine Total Care Anticavity Mouthwash

Restores enamel
Helps prevent cavities
Helps kill germs that cause bad breath
Freshens breath

IMPORTANT: Read directions for proper use.

Sealed with printed neckband for your protection

1L (33.8 FL OZ)

163.004/163AE

INGREDIENTS AND APPEARANCE

ANTICAVITY  
sodium fluoride mouthwash

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55301-163
Route of Administration	ORAL

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)
ALCOHOL (UNII: 3K9958V90M)
POLOXAMER 407 (UNII: TUF2IVW3M2)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
PHOSPHORIC ACID (UNII: E4GA8884NN)
SODIUM PHOSPHATE (UNII: SE337SVY37)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55301-163-86	1 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/29/2006

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part355	01/29/2006

Labeler - Your Military Exchanges (001695568)

Registrant - Vi-Jon, Inc (088520668)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc		088520668	manufacture(55301-163)