AHUIFT WART REMOVER- salicylic acid 17% wart remover ointment

AHUIFT Wart Remover by

Drug Labeling and Warnings

AHUIFT Wart Remover by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei 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 health 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，Chlorhexidine

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AHUIFT WART REMOVER 
salicylic acid 17% wart remover ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-081
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
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
BORNEOL (UNII: M89NIB437X)
CHLORHEXIDINE (UNII: R4KO0DY52L)
METHYLPARABEN (UNII: A2I8C7HI9T)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-081-01	30 g in 1 TUBE; Type 0: Not a Combination Product	02/26/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	02/26/2025

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-081)