SOUTH MOON TAG UND MUTTERMALEN FERNUNGSPFLASTER- glycerin patch

SOUTH MOON Tag Und Muttermalen Fernungspflaster by

Drug Labeling and Warnings

SOUTH MOON Tag Und Muttermalen Fernungspflaster by is a Otc medication manufactured, distributed, or labeled by Guangdong Ouhoe Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

APIS MELLIFERA VENOM,TEA LEAF OIL,TOCOPHEROL

purpose

Painless removal of skin warts and moles; fast removal of skin tags; removal of many types of warts.

use

Tear off the patch and stick it on the corresponding skin location where warts and moles grow, leave it for a few hours and then tear it off.

WARNINGS

Please keep out of reach of children. Do not swallow.Pleasel clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place.

Do not use

Discontinue use if signs of irritation or rash occur.

Stop use

Discontinue use if signs of irritation or rash occur.

KEEP OUT OF REACH OF CHILDREN

Please keep out of reach of children. Do not swallow.

STORAGE AND HANDLING

Store in a cool and dry place.

INACTIVE INGREDIENT

SALICYLIC ACID、GLYCERIN

INDICATIONS & USAGE

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOUTH MOON TAG UND MUTTERMALEN FERNUNGSPFLASTER 
glycerin patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84744-051
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8)	TOCOPHEROL	21.6 mg  in 144 mg
TEA LEAF OIL (UNII: VC855RRT77) (TEA LEAF OIL - UNII:VC855RRT77)	TEA LEAF OIL	14.4 mg  in 144 mg
APIS MELLIFERA VENOM (UNII: 76013O881M) (APIS MELLIFERA VENOM - UNII:76013O881M)	APIS MELLIFERA VENOM	43.2 mg  in 144 mg

Inactive Ingredients
Ingredient Name	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ)	21.6 mg  in 144 mg
GLYCERIN (UNII: PDC6A3C0OX)	36 mg  in 144 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84744-051-01	144 mg in 1 BOX; Type 0: Not a Combination Product	10/21/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	10/21/2024

Labeler - Guangdong Ouhoe Biotechnology Co., Ltd. (843651433)

Registrant - Guangdong Ouhoe Biotechnology Co., Ltd. (843651433)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Ouhoe Biotechnology Co., Ltd.		843651433	manufacture(84744-051)