QSOOWIS WART CORN REMOVER- salicylic acid 40% wart corn remover patch

QSOOWIS WART CORN REMOVER by

Drug Labeling and Warnings

QSOOWIS WART CORN 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 40%

Purpose

Wart and Corn Remover

Use

For the removal of warts and corns.

Warnings

For external use only.

Do not use

On irritated,infected, or reddened skin; on genital warts or warts on the face; on moles, birthmarks, or warts with hair growing from them;on mucous mempranes.

When Using

Avoid contact with eyes or face. If the product gets into the eyes, rinse thoroughly with water.

Stop Use

Stop use and ask a doctor if discomfort persists or worsens

Ask Doctor

Ask a doctor if you have diabetes or poor blood circulation.

Keep Out Of Reach Of Children

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

Directions

Wash the affected area thoroughly with warm water. (Optional: soak the wart in warm water for 5 minutes.)Dry the area thoroughly. lf needed, cut the plaster to fit the wart. Apply the medicated plaster. Repeat every 48 hours as needed, for up to 12 weeks.Other information: Store between 59°F and 86°F(15°C and 30°C).

Inactive ingredients

hard paraffin,lanolin,phenol, petrolatum

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

QSOOWIS WART CORN REMOVER 
salicylic acid 40% wart corn remover patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-141
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	40 g  in 100

Inactive Ingredients
Ingredient Name	Strength
PARAFFIN (UNII: I9O0E3H2ZE)
PHENOL (UNII: 339NCG44TV)
PETROLATUM (UNII: 4T6H12BN9U)
LANOLIN (UNII: 7EV65EAW6H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-141-01	30 in 1 BOX; Type 0: Not a Combination Product	07/07/2025
2	NDC: 84010-141-02	42 in 1 BOX; Type 0: Not a Combination Product	07/07/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	07/07/2025

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

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-141)