FOASU JIN POWDERWASH- allantoin, panthenol powder

FOASU JIN POWDERWASH by

Drug Labeling and Warnings

FOASU JIN POWDERWASH by is a Otc medication manufactured, distributed, or labeled by HANSCOS Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

allantoin, panthenol

Purpose

skin protectant

Use

apply proper amount to the skin, or the enclosed bubble pad, wet it with water, make enough bubbles, massage gently all over the face, and rinse thoroughly with warm water

Warnings

For external use only

1) Please consult your doctor if you experience side effects such as swelling, itching, or reddening on the area where you applied this product

2) Do not apply on wounds or cuts. 3) Do not store where children may reach, and avoid keeping it exposed to direct sunlight.

Directions

for external use only

Inactive ingredients

ZEA MAYS (CORN) STARCH
SODIUM LAUROYL GLUTAMATE
SODIUM COCOYL GLUTAMATE
MANNITOL
BETAINE
PAPAIN
CELLULOSE GUM
ARTEMISIA VULGARIS EXTRACT
ETHYLHEXYLGLYCERIN
CENTELLA ASIATICA EXTRACT
CENTELLA ASIATICA EXTRACT
BROMELAIN
DISODIUM EDTA
ANGELICA GIGAS ROOT EXTRACT
BLETILLA STRIATA ROOT EXTRACT
PORIA COCOS EXTRACT
ANGELICA TENUISSIMA ROOT EXTRACT
POLYGONATUM OFFICINALE RHIZOME/ROOT EXTRACT
CNIDIUM OFFICINALE ROOT EXTRACT
ECTOIN
BUTYLENE GLYCOL
WATER
1,2-HEXANEDIOL
PEARL POWDER

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FOASU JIN POWDERWASH 
allantoin, panthenol powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77964-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.1 g  in 100 g
PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z)	PANTHENOL	0.01 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77964-005-01	70 g in 1 CONTAINER; Type 0: Not a Combination Product	02/27/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/27/2022

Labeler - HANSCOS Co.,Ltd. (688494423)

Registrant - HANSCOS Co.,Ltd. (688494423)

Establishment
Name	Address	ID/FEI	Business Operations
HANSCOS Co.,Ltd.		688494423	manufacture(77964-005)