NEKVNRO WART REMOVER- wart remover liquid

Nekvnro Wart Remover by

Drug Labeling and Warnings

Nekvnro Wart Remover by is a Otc medication manufactured, distributed, or labeled by Guoyu Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Salicylic acid 5%

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

and ask a doctor if
discomfort persists.

Ask Doctor

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
·avoid excessive heat 37°C (99°F)
·skin discoloration may accur during or after use
·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 
wart remover liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84844-013
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
BORNEOL (UNII: M89NIB437X)
PODOFILOX (UNII: L36H50F353)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84844-013-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/07/2024
2	NDC: 84844-013-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/07/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	11/07/2024

Labeler - Guoyu Trading Co., Ltd. (963348600)

Establishment
Name	Address	ID/FEI	Business Operations
Guoyu Trading Co., Ltd.		963348600	manufacture(84844-013)