ANTISPETIC- eucalyptol, menthol, methyl salicylate, thymol mouthwash 
Target Corporation

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 ingredients

Eucalyptol 0.092%

Menthol 0.042%

Methyl salicylate 0.060%

Thymol 0.064%

Purpose

Antigingivitis, antiplaque

Use

help control plaque that leads to gingivitis

Warnings for this product

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

other information

cold weather may cloud this product. Its antiseptic properties are not affected. Store at room temperature (59°-77°F).

Inactive ingredients

water, alcohol 21.6%, sorbitol solution, flavor, poloxamer 407, benzoic acid, sodium saccharin, sodium benzoate, FD&C green no.3

Disclaimer

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

ADA Council Statement

The ADA Council on Scientific Affairs Acceptance of UP & UP blue mint antiseptic mouthwash is based on its finding that the product is efective in helping to prevent and reduce gingivitis and plaque above the gumline, when used as directed.

Adverse Reactions

Distributed by Target Corporation

Minneapolis, MN 55403

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

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SAFETY SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION

ADA

Accepted

American

Dential

Association

antiseptic

mouthwash

Kills germs that cause bad breath, plaque and the gum disease gingivitis

Compare to Listerine Antiseptic Cool Mint

BLUE MINT FLAVOR

up & up

50.7 FL OZ (1.5 L)

image description

ANTISPETIC 
eucalyptol, menthol, methyl salicylate, thymol mouthwash
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-664
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EUCALYPTOL (UNII: RV6J6604TK) (EUCALYPTOL - UNII:RV6J6604TK) EUCALYPTOL 0.92 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.42 mg  in 1 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 0.60 mg  in 1 mL
THYMOL (UNII: 3J50XA376E) (THYMOL - UNII:3J50XA376E) THYMOL 0.64 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
SORBITOL (UNII: 506T60A25R)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11673-664-12 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/11/1993
2 NDC:11673-664-77 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/11/1993
3 NDC:11673-664-19 94 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/11/1993
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part356 08/11/1993
Labeler - Target Corporation (006961700)
Registrant - Vi-Jon (790752542)
Establishment
Name Address ID/FEI Business Operations
Vi-Jon 790752542 manufacture(11673-664)

Revised: 5/2017
Document Id: 9ab2353f-2325-4c85-9590-7e2aea72fabd
Set id: 55e29b2f-a51f-4473-a022-aa9b921beb87
Version: 4
Effective Time: 20170517
 
Target Corporation