HEALMUSZ WART REMOVER- salicylic acid 10% wart remover liquid

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

Salicylic acid 10% 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 on the surface.
·the plantar wart is recognized by its location only on
the bottom of the foot, its tenderness
and interruption of the footprint pattern

Warnings

For external use only.
Keep away from fire and flame.

Do not use

on irritated skin or on any area that is infected or reddened
·on moles, 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

·avoid contact with eyes.
If product gets into the eye, flush with water for 15 minutes.
·avoid inhaling vapors
·cap tightly and store at room temperature away from heat

Stop Use

Stop use and ask a doctor if discomfort persists.

Ask Doctor

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.

Directions

wash affected area·may soak wart in warm water for 5 minutes· Use a cotton swab to apply a sufficient amount to cover each wart. Let it dry.repeat this procedure once or twice daily as needed (until wart is removed)for up to 12 weeks

Other information

store at room
temperature·avoid excessive heat
37°C (99°F)·skin discoloration may
accur during or after use

Inactive ingredients

Ethanol, Phenoxyethanol,Polyethylene glycol‑400

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HEALMUSZ WART REMOVER 
salicylic acid 10% wart remover liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87686-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87686-002-01	30 g in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	05/12/2026

Labeler - Jiangxi Zhongletang Pharmaceuticals Co.,Ltd. (411295811)