WART SKIN TAG REMOVER- salicylic acid liquid

WART SKIN TAG REMOVER by

Drug Labeling and Warnings

WART SKIN TAG REMOVER by is a Otc medication manufactured, distributed, or labeled by Guangzhou ChuanMa International Trading Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

SALICYLIC ACID 15.00%
LACTIC ACID 4.50%

PURPOSE

Wart remover

WHEN USING

When using this product:e avoidcontact with eyes. lf the product gets intothe eye,flush with water for 15 minutes avoid inhaling vapors o cap the bottletightly e out of direct sunlight and storeat room temperature away from heat

DOSAGE & ADMINISTRATION

wash the affected areamay soak the wart in warm water for 5minutes e dry area thoroughly e usingthe applicator(brush or cotton swab), applyone drop at a time to sufficiently cover eachwart e allow it to fully absorb and let dryrepeat this procedure once or twicedaily as needed (until the wart is removed)for up to 12 weeks

INDICATIONS & USAGE

for the removal of common andplantar warts o the common wart is easilyrecognized by the rough"cauliflower-like"appearance of the surface o the plantarwart is recognized by its location only onthe bottom of the foot,its tenderness andthe interruption of the footprint pattern

WARNINGS

WarningsFor external use only.keep away from fire and flame.only use on affected area.

DO NOT USE

Do not use: on irritated skin or on anyarea that is infected or reddened o onmoles, birthmarks, warts with hair growingfrom them, warts on the face or mucousmembranes

KEEP OUT OF REACH OF CHILDREN

keep out of reachof children, if swallowed, get medical helpor contact a Poison Control Center rightaway.

INACTIVE INGREDIENT

Inactive ingredients: ®Alcohol, Propylene Glycol, Water, PentyleneGlycol, Oleth-20, Peg-40 HydrogenatedCastor Oil, Cymbopogon Citratus Leaf Oil,Polyethylene Glycol 400

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WART SKIN TAG REMOVER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85593-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	15 g  in 100 mL
LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT)	LACTIC ACID	4.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CYMBOPOGON CITRATUS LEAF OIL (UNII: 5BIA40E9ED)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
WATER (UNII: 059QF0KO0R)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
OLETH-20 (UNII: YTH167I2AG)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85593-101-01	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/20/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	07/20/2025

Labeler - Guangzhou ChuanMa International Trading Co.,Ltd. (510247477)

Registrant - Guangzhou ChuanMa International Trading Co.,Ltd. (510247477)