WART REMOVER LIQUID liquid

Wart Remover Liquid by

Drug Labeling and Warnings

Wart Remover Liquid by is a Otc medication manufactured, distributed, or labeled by Premier Brands of America Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 17%w/w

Purpose

Wart remover

Use

• for the removal of common and plantar warts. The common wart is easily recognized by the rough 'cauliflower-like' appearance of the surface. Plantar wart is recognized by its location only on the bottom of the foot, its tenderness and the interruption of the footprint pattern.

Warnings

For external use only.

Flammable

• keep away from fire or flame
• cap bottle tightly and store at room temperature away heat

Do not use

if you are a diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist

Do not use on

• irritated, infected or reddened skin
• genital warts and warts on the face
• moles, birthmarks and warts with hair growing from them
• mucous membranes

When using this product

• avoid contact with eyes. If product gets into the eyes, flush with water for 15 minutes
• avoid inhaling vapors

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• wash affected area, may soak wart in warm water for 5 minutes
• dry area thoroughly
• apply small amount of wart remover with applicator to sufficiently cover each wart
• let dry and repeat this procedure once or twice daily until wart is removed for up to 12 weeks

Other information

store between 20°C to 30°C (68°F to 86°F)

Inactive ingredients

camphor, castro oil, ethanol, ethyl ether, nitrocellulose

Questions?

Call 1-866-964-0939

Principal Display Panel

Premier

Miximum Strength

LIQUID WART REMOVER

MEDICATED

SALICYLIC ACID

• Removes common and plantar wart
• Convenient applicator
• safe and Effective

NET WT 0.31 Fl. Oz (9mL)

INGREDIENTS AND APPEARANCE

WART REMOVER LIQUID 
wart remover liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56104-025
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.17 g  in 9 mL

Inactive Ingredients
Ingredient Name	Strength
PYROXYLIN (UNII: KYR8BR2X6O)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
CASTOR OIL (UNII: D5340Y2I9G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 56104-025-09	9 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	10/28/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358B	10/28/2015

Labeler - Premier Brands of America Inc. (080051232)