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 Shenzhen Xingqi Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

TALC 1%

PURPOSE

wart removal

USES

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

warning

1, external use,Avoid contact with eyes and mouth.
2,If irritation or abnormality occurs, stop using and wash with water
3, Please keep this product out of the reach of children

Dosage and administration

For external use only.

Do not use

1, external use, Avoid contact with eyes and mouth.
2,lf irritation or abnormality occurs, stop using and wash with water
3, Please keep this product out of the reach of children

When using section

1, external use,Avoid contact with eyes and mouth.
2,lf irritation or abnormality occurs, stop using and wash with water
3, Please keep this product out of the reach of children

STOP USE

1, external use, Avoid contact with eyes and mouth.
2,lf irritation or abnormality occurs, stop using and wash with water
3, Please keep this product out of the reach of children

KEEP OUT OF REACH OF CHILDREN

Please keep this product out of the reach of children

INACTIVE INGREDIENT

POTASSIUM ALUM , SODIUM ALGINATE

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: 84613-052
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TALC (UNII: 7SEV7J4R1U) (TALC - UNII:7SEV7J4R1U)	TALC	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM ALUM (UNII: 1L24V9R23S)	1 g  in 100 g
SODIUM ALGINATE (UNII: C269C4G2ZQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84613-052-01	30 g in 1 BOX; Type 0: Not a Combination Product	08/08/2024

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

Labeler - Shenzhen Xingqi Technology Co., Ltd. (974493783)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Xingqi Technology Co., Ltd.		974493783	manufacture(84613-052)