FAST NATURAL WART REMOVAL- salicylic acid 17% ointment

FAST NATURAL WART REMOVAL by

Drug Labeling and Warnings

FAST NATURAL WART REMOVAL by is a Otc medication manufactured, distributed, or labeled by Shenzhen Haizhida E-commerce Co., Ltd, Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 17%

PURPOSE

Wart remover

INDICATIONS & USAGE

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

WARNINGS

For external use only- Avoid contact with eyes.
lf 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.
lf you are diabetic or have poor blood circulation.
On birthmarks, warts with hair growth,or moles.

WHEN USING

lf pregnant or breastfeeding, consult a health professional before use.

STOP USE

discomfort persists.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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 INGREDIENT

Water
Polyethylene Glycol
Glycerin
Borneol
Methylparaben
Chlorhexidine

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FAST NATURAL WART REMOVAL 
salicylic acid 17% ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85825-001
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)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
BORNEOL (UNII: M89NIB437X)
CHLORHEXIDINE (UNII: R4KO0DY52L)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85825-001-01	1 in 1 BOX	06/23/2025
1		20 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	06/23/2025

Labeler - Shenzhen Haizhida E-commerce Co., Ltd (509640283)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(85825-001)