WART REMOVER (SALICYLIC ACID) LIQUID- salicylic acid liquid

WART REMOVER (salicylic acid) liquid by

Drug Labeling and Warnings

WART REMOVER (salicylic acid) liquid by is a Otc medication manufactured, distributed, or labeled by Shenzhen Finona Information Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 5%

PURPOSE

Wart remover

INDICATIONS & USAGE

.To remove warts such as plantar wart, flatwart. common wart and corns, calluses.
.The plantar wart is recognized by it location only on the bottom of the foot it's tenderness, and the interruption of the footprint pattern.

WARNINGS

The liquid can get easily volatilized & crystalllzed, tighten the cap after use.
Avoid long-term contact with alr while using.
For external use only,don't contact with eyes or swallow, Children should use it under the supervision of adults.

DO NOT USE

.On damaged skin(cuts.abrasions,eczema, sunburn.
.lf you are allergic to any of the ingredients in this product.
.lf you are pregnant or breastfeeding,

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

.Wash the affected area.
.May soak the wart in warm water for 5 minutes.
.Dry area thoroughly.
.Using the applicator(cotton swab),apply a layer of ointment to sufficiently cover each wart.
.Allow it to fully absorb and cover it with a bandage as needed.
.Repeat this procedure once or twice daily as needed (until the wart is removed) for up to 12 weeks.

INACTIVE INGREDIENT

Shard paraffin
lanolin
phenol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WART REMOVER (SALICYLIC ACID) LIQUID 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85839-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.05 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PARAFFIN (UNII: I9O0E3H2ZE)
LANOLIN (UNII: 7EV65EAW6H)
PHENOL (UNII: 339NCG44TV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85839-003-01	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/26/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	06/26/2025

Labeler - Shenzhen Finona Information Technology Co., Ltd (511271543)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Finona Information Technology Co., Ltd		511271543	manufacture(85839-003)