QSOOWIS WART REMOVER- salicylic acid 17% wart remover liquid

QSOOWIS WART REMOVER by

Drug Labeling and Warnings

QSOOWIS 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% V/V

Purpose

Wart remover

Use

·for the removal of common and plantar warts

·the common wart is easily recognized by the rough “cauliflower-like” appearance on the surface.

·the plantar wart is recognized by its location only on the bottom of the foot, its tenderness and interruption of the foot print pattern

Warnings

For external use only. Flammable.

Keep away from fire and flame.

Do not use

on irritated skin or on any area that is infected or reddened

·on moles, birthmarks, warts with hair growing from them, genital warts or warts on the face or mucous membranes.
·if you have diabetes or poor blood circulation.

When Using

avoid contact with eyes.
If product gets into the eye, flush with water for 15 minutes.

·avoid inhaling vapors·cap tightly and store at room temperature away from heat

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, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

·wash affected area·may soak wart in warm water for5 minutes
·use a cotton swab to apply a sufficient amount to cover each wart.let it dry.
·repeat this procedure once or twice daily as needed (until wart is removed) for up to 12 weeks

Other information

store at room temperature
·avoid excessive heat 37°C (99°F)

·skin discoloration may accur during or after use.

Inactive ingredients

Water，Borneol，Glycerin，Podofilox，Polyethylene Glycol， etc.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

QSOOWIS WART REMOVER 
salicylic acid 17% wart remover liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-050
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 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
PODOFILOX (UNII: L36H50F353)
BORNEOL (UNII: M89NIB437X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-050-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/25/2024
2	NDC: 84010-050-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/25/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	11/25/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-050)