FOASU JIN POWDERWASH- allantoin, panthenol powder 
HANSCOS Co.,Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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

label

FOASU JIN POWDERWASH 
allantoin, panthenol powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77964-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.1 g  in 100 g
PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL0.01 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77964-005-0170 g in 1 CONTAINER; Type 0: Not a Combination Product02/27/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/27/2022
Labeler - HANSCOS Co.,Ltd. (688494423)
Registrant - HANSCOS Co.,Ltd. (688494423)
Establishment
NameAddressID/FEIBusiness Operations
HANSCOS Co.,Ltd.688494423manufacture(77964-005)

Revised: 2/2022
Document Id: d8fa5b99-b9ab-fb14-e053-2a95a90a74d9
Set id: d8fa5b99-b9aa-fb14-e053-2a95a90a74d9
Version: 1
Effective Time: 20220227
 
HANSCOS Co.,Ltd.