LISTERINE ULTRACLEAN FRESH CITRUS- eucalyptol, menthol, unspecified form, methyl salicylate, and thymol mouthwash

Listerine Ultraclean Fresh Citrus by

Drug Labeling and Warnings

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

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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, Yellow 6, Red 40

Questions ?

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

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 1.5 L Bottle Label

ANTISEPTIC
LISTERINE®
ULTRACLEAN

FOR UP TO A 3X
LONGER LASTING
CLEAN FEELING*

*vs. brushing alone

FRESH CITRUS

1.5L (1 Qt 1 Pt 2.7 Fl Oz)

INGREDIENTS AND APPEARANCE

LISTERINE ULTRACLEAN FRESH CITRUS 
eucalyptol, menthol, unspecified form, methyl salicylate, and thymol mouthwash

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0398
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)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0398-1	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/10/2012
2	NDC: 69968-0398-2	1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/10/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part356	08/10/2012

Labeler - Johnson & Johnson Consumer Inc. (002347102)