QQE WART REMOVER- salicylic acid liquid

QQE WART REMOVER by

Drug Labeling and Warnings

QQE WART REMOVER by is a Otc medication manufactured, distributed, or labeled by Hainan Shengtaizhuo International Information Development Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

WART REMOVER

ACTIVE INGREDIENT

20% SALICYLIC ACID

INDICATIONS & USAGE

1. Clean the affected area.
2. Dip a cotton swab in a small amount of the liquid medicine and apply it only to the surface of the wart, avoiding contact with the surrounding skin.
3. You can apply moisturizing cream around the wart.
4. Let it air dry naturally after application and avoid friction or covering with clothing.

WARNINGS

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

KEEP OUT OF REACH OF CHILDREN

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

WHEN USING

1. Do not apply on other parts of the body, For topical use only on the scalp
2. Avoid contact with the eyes in case of accidental contact rinse eyes with large arnounts of cool tap water.

DO NOT USE

You are under 18 years old. Do not use it for infants and children. Red, inflamed, infected, itchy or painful scalp.
You are using other medications on the affected area. If you have heart disease, consult your doctor before using.

STOP USE

Chest pain, rapid heart beat, faintness, or dizziness occurs sudden, unexplained weight gain occurs,your hands or feet swell.

DOSAGE & ADMINISTRATION

Twice each day,4 sprays (1ml)each time. 30 days supply

INACTIVE INGREDIENT

WATER, BORNEOL, GLYCERIN, PODOFILOX, POLYETHYLENE GLYCOL, BISABOLOL, ALLANTOIN.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

QQE WART REMOVER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84556-425
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
BORNEOL (UNII: M89NIB437X)
GLYCERIN (UNII: PDC6A3C0OX)
PODOFILOX (UNII: L36H50F353)
WATER (UNII: 059QF0KO0R)
ALLANTOIN (UNII: 344S277G0Z)
BISABOLOL (UNII: 24WE03BX2T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84556-425-01	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/06/2025	09/29/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	10/06/2025	09/29/2026

Labeler - Hainan Shengtaizhuo International Information Development Co., LTD (976885514)

Establishment
Name	Address	ID/FEI	Business Operations
Hainan Shengtaizhuo International Information Development Co., LTD		976885514	label(84556-425)