ANTISEPTIC MOUTH RINSE  - eucalyptol, menthol, methyl salicylate and thymol mouthwash 
Vi-Jon

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Drug Facts

Active ingredients
Eucalyptol 0.092%, Menthol 0.042%
Methyl salicylate 0.060%, Thymol 0.064%

Purpose
Antiginvitis, Antiplaque

Use helps control plaque that leads to gingivitis

Warnings

Do not use if you have painful or swollen gums, pus from the gum line, loose teeth or increased spacing between the teeth.  See your dentist immediately.  These may be signs of periodontitis, a serious form of gum disease.

Stop use and ask a dentist if gingivitis, bleeding, or redness persists for more than 2 weeks

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 12 years of age and older - vigorously swish 20 mL (2.3 FL OZ or 4 teaspoonfuls) between teeth for 30 seconds then spit out: do not swallow

children under 12 years of age - consult a dentist or doctor

• this rinse is not intended to replace brushing or flossing

Other information cold weather may cloud this product.  Its antiseptic properties are not affected.  Store at room temperature (59⁰-77⁰F)

Inactive ingredients water, alcohol 26.9%, benzoic acid, poloxamer 407, sodium benzoate, caramel

The ADA Council on Scientific Affairs' Acceptance of Swan Original Antiseptic Mouthrinse is based on the finding that the
product is effective in helping to prevent and reduce gingivitis and plaque above the gumline, when used as directed.

This product is not manufactured or distributed by Johnson + Johnson Healthcare Products, distributor of Listerine.

DSP-TN-15000
DSP-MO-34
SDS-TN-15012

Distributed by: Vi-Jon, One Swan Drive, Smyrna, TN 37167

Sealed With Printed Neckband For Your Protection

ANTISEPTIC
Mouth Rinse
original
Kills Germs that
Cause Bad Breath
Plaque + the Gum
Disease Gingivitis

Compare to the active ingredients of Listerine

1.5 LITERS (50.7 FL OZ)

ADA
Accepted
American
Dental
Association

ANTISEPTIC MOUTH RINSE  eucalyptol   mouthwash

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 0869-0318 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTOL (EUCALYPTOL) EUCALYPTOL .092 kg  in 100 L MENTHOL (MENTHOL) MENTHOL .042 kg  in 100 L METHYL SALICYLATE (METHYL SALICYLATE) METHYL SALICYLATE .060 kg  in 100 L THYMOL (THYMOL) THYMOL .064 kg  in 100 L

Inactive Ingredients Ingredient Name Strength WATER   ALCOHOL   BENZOIC ACID   POLOXAMER 407   CARAMEL

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0869-0318-86 1 L In 1 BOTTLE, PLASTIC None 2 0869-0318-69 .25 L In 1 BOTTLE, PLASTIC None 3 0869-0318-12 1.5 L In 1 BOTTLE, PLASTIC None 4 0869-0318-13 1.25 L In 1 BOTTLE, PLASTIC None 5 0869-0318-77 .5 L In 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part356	07/15/1989

Labeler - Vi-Jon (790752542)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Operations
Vi-Jon		790752542	manufacture

Revised: 01/2011Vi-Jon