WART REMOVER- salicylic acid liquid

Wart remover by

Drug Labeling and Warnings

Wart remover by is a Otc medication manufactured, distributed, or labeled by Hengyang Chuangjiujia Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Wart remover

ACTIVE INGREDIENT

Salicylic acid 10%

PURPOSE

Wart remover

INDICATIONS & USAGE

for the removal of common and plantar warts ·the commonwart is easilyrecognized by the rough “cauliflower-like” appearance on the surface. the plantar wart is recognized by its location only on thebottom of the foot, its tenderness and interruption of the footprint pattern

WARNINGS

For externaluse only.Flammable.

DO NOT USE

Do not use on irritated skin or on any area that is infected orreddened·birthmarks, warts with hair growing from them,genital warts or warts on the face or mucous membranes
if you have diabetes or poor blood circulation.

WHEN USING

When using this product·avoid contact with eyes. lf productgets into the eye, flush with water for 15 minutes. avoid inhalingvapors. cap tightly and store at room temperature away from heat

STOP USE

Stop use and ask a doctor if
discomfort persists.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center(1-800-222-1222)right away.

DOSAGE & ADMINISTRATION

Directions·wash affected area may soak wart in warm waterfor 5 minutes·

dry area thoroughly·by squeezing tube gently, apply onedrop at a time to sufficiently cover each wart·let dry.

repeat this procedure once or twice daily as needed (untiwart is removed) for up to 12 weeks

STORAGE AND HANDLING

Other information·store at room temperature avoidexcessive heat 37°℃ (99°F)·skin discoloration may accurduring or after use wipe the tip of the tube with a papertowel between uses

INACTIVE INGREDIENT

Borneol
Glycerin
Podofilox
Polyethylene
Glycol
Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WART REMOVER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84735-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.1 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PODOFILOX (UNII: L36H50F353)
POLYETHYLENE (UNII: UG00KM4WR7)
BORNEOL (UNII: M89NIB437X)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCOL (UNII: FC72KVT52F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84735-002-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/30/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	12/30/2024

Labeler - Hengyang Chuangjiujia Trading Co., Ltd. (977292157)

Establishment
Name	Address	ID/FEI	Business Operations
Hengyang Chuangjiujia Trading Co., Ltd.		977292157	manufacture(84735-002)