NEKVNRO WART REMOVER PATCH- wart remover patch patch

Nekvnro Wart Remover Patch by

Drug Labeling and Warnings

Nekvnro Wart Remover Patch 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 1%

Purpose

Anti-inflammatory and analgesic

Use

Wart removal patch can reduce inflammation, relieve pain and soften cuticles.

Warnings

external use,Avoid contact with eyes and mouth.

Do not use

if irritation or abnormality occurs, stop using and wash with water.

When Using

Avoid contact with eyes and mouth,if irritation or abnormality occurs, stop using and wash with water,Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop Use

Avoid contact with eyes and mouth,if irritation or abnormality occurs, stop using and wash with water.

Ask Doctor

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

Keep Oot Of Reach Of Children

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

Directions

lean and wipe the skin around the wart，Remove the wart removal tablet.Apply it to the wart,Cover it completely，1capsule can last for 8-12 hours, Recommended 2-3 times a day.

Inactive ingredients

Hydrocolloid,Cellulose Gum,Polyisobutylene,Polyisobutylene，Cyperus rotundus，Prunella vulgaris.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEKVNRO WART REMOVER PATCH 
wart remover patch patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84844-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	1 g  in 100

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE GUM (UNII: K679OBS311)
CYPERUS PROLIFER WHOLE (UNII: V5C409ED5L)
PRUNELLA VULGARIS (UNII: Y45L13XZ2U)
POLYISOBUTYLENE (1100000 MW) (UNII: FLT10CH37X)
1-DODECYLPERHYDROAZEPINE-1-OXIDE (UNII: E9FWJ87VG7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84844-002-01	216 in 1 BOX; Type 0: Not a Combination Product	10/23/2024
2	NDC: 84844-002-02	360 in 1 BOX; Type 0: Not a Combination Product	10/23/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	10/23/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Guoyu Trading Co., Ltd.		963348600	manufacture(84844-002)