HEALMUSZ FAST NATURAL WART REMOVAL- salicylic acid 17% fast natural wart removal ointment

HEALMUSZ FAST NATURAL WART REMOVAL by

Drug Labeling and Warnings

HEALMUSZ FAST NATURAL WART REMOVAL by is a Otc medication manufactured, distributed, or labeled by Jiangxi Yudexi Pharmaceutical Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic acid 17%

Purpose

Wart remover

Use

For the removal of common warts, which have a rough,cauliflower-like appearance.

Warnings

For external use only- Avoid contact with eyes. If the product gets into eyes, rinse with water for 15 minutes. Avoid inhaling vapors.

Do not use

On irritated or infected skin, or reddened areas. If you are diabetic or have poor blood circulation. On birthmarks, warts with hair growth,or moles.

When Using

If pregnant or breastfeeding, consult a healthcare professional before use.

Stop Use

Stop use and ask a doctor if discomfort persists.

Ask Doctor

Stop use and ask a doctor if discomfort persists.

Keep Oot Of Reach Of Children

If swallowed, seek immediate medical help or contact a Poison Control Center.

Directions

1.Wash the affected area.(Soaking in warm water for 5 minutes may help.)
2. Dry thoroughly. 3. Apply a small amount to cover each wart. Let it dry 4. Repeat twice daily as needed, for up to 12 weeks.

Inactive ingredients

Water, Polyethylene Glycol, Glycerin, Borneol，Methylparaben.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HEALMUSZ FAST NATURAL WART REMOVAL 
salicylic acid 17% fast natural wart removal ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-061
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	17 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
BORNEOL (UNII: M89NIB437X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-061-01	20 g in 1 TUBE; Type 0: Not a Combination Product	02/07/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	02/07/2026

Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)