LISTERINE ULTRACLEAN ARCTIC MINT- eucalyptol, menthol, unspecified form, methyl salicylate, and thymol mouthwash

Listerine Ultraclean Arctic Mint by

Drug Labeling and Warnings

Listerine Ultraclean Arctic Mint by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredients

Eucalyptol(0.092%)
Menthol (0.042%)
Methyl Salicylate (0.060%)
Thymol (0.064%)

Purposes

Antiplaque/antigingivitis

Uses

helps prevent and reduce:

• Plaque
• gingivitis

Warnings

Do not use in children under 12 years of age

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

• rinse full strength for 30 seconds with 20 mL (2/3 fluid ounce or 4 teaspoonfuls) morning and night
• do not swallow

Other information

• store at room temperature
• cold weather may cloud this product. Its antiseptic properties are not affected.

Inactive ingredients

Water, Alcohol(21.6%), Sorbitol, Poloxamer 407, Flavor, Benzoic Acid, Zinc Chloride, Sodium Benzoate, Sucralose, Sodium Saccharin, Blue 1

Questions ?

Call toll free 888-222-0182 or 215-273-8755 (collect)

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Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

ANTISEPTIC
LISTERINE®
ULTRACLEAN

FOR UP TO A 3X
LONGER LASTING
CLEAN FEELING*

*vs. brushing alone

ARCTIC MINT®

500 mL (1.05 Pt)

INGREDIENTS AND APPEARANCE

LISTERINE ULTRACLEAN ARCTIC MINT 
eucalyptol, menthol, unspecified form, methyl salicylate, and thymol mouthwash

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0399
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, Unspecified Form (UNII: L7T10EIP3A) (Menthol, Unspecified Form - UNII:L7T10EIP3A)	Menthol, Unspecified Form	0.42 mg  in 1 mL
Methyl Salicylate (UNII: LAV5U5022Y) (Salicylic Acid - UNII:O414PZ4LPZ)	Methyl Salicylate	0.6 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)
Zinc Chloride (UNII: 86Q357L16B)
Sodium Benzoate (UNII: OJ245FE5EU)
Sucralose (UNII: 96K6UQ3ZD4)
Saccharin Sodium (UNII: SB8ZUX40TY)
FD&C Blue No. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0399-3	95 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/03/2012
2	NDC: 69968-0399-8	250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/03/2012
3	NDC: 69968-0399-9	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/03/2012
4	NDC: 69968-0399-1	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/03/2012
5	NDC: 69968-0399-2	1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/03/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part356	07/03/2012

Labeler - Johnson & Johnson Consumer Inc. (002347102)