NEKVNRO WART REMOVER- salicylic acid wart remover liquid

NeKvnro WART REMOVER by

Drug Labeling and Warnings

NeKvnro 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 5% w/w

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 footprint 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 for 5 minutes
·dry area thoroughly·by squeezing tube gently, apply one drop at a time to sufficiently cover each wart·let 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.skin discoloration may accur during or after use*avoid excessive heat 37°C (99°F)*wipe the tip of the tube with a paper towel between uses

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEKVNRO WART REMOVER 
salicylic acid wart remover liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-024-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/18/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	08/18/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-024)