FOASU JIN POWDERWASH

Manufacturer: HANSCOS Co.,Ltd.
Effective date: 2022-02-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:48:32

Label at a glance#

ProductFOASU JIN POWDERWASH

Active ingredientALLANTOIN, PANTHENOL

Label structure8 sections

Dosage and administration

for external use only

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

allantoin, panthenol

Purpose

OTC - PURPOSE SECTION

skin protectant

Use

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

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

DOSAGE & ADMINISTRATION SECTION

for external use only

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77964-005-01	FOASU JIN POWDERWASH	70 g in 1 CONTAINER	POWDER	70		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77964-005	FOASU JIN POWDERWASH (ALLANTOIN, PANTHENOL) POWDER [HANSCOS CO.,LTD.]	1	Current NDC, Legacy NDC, 1 package rows	20220227_d8fa5b99-b9aa-fb14-e053-2a95a90a74d9.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

FOASU JIN POWDERWASH
allantoin, panthenol
WATER
BUTYLENE GLYCOL
ALLANTOIN
PANTHENOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77964-005	77964-005-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
ALLANTOIN	344S277G0Z	ACTIB
PANTHENOL	WV9CM0O67Z	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
FOASU JIN POWDERWASH	ALLANTOIN, PANTHENOL	HANSCOS Co.,Ltd.	d8fa5b99-b9aa-fb14-e053-2a95a90a74d9	2022-02-27	Warnings	Exact identifier ndc (package): 77964-005-01 ndc (product): 77964-005 ndc11 (package): 77964000501 spl id: d8fa5b99-b9ab-fb14-e053-2a95a90a74d9 spl set id: d8fa5b99-b9aa-fb14-e053-2a95a90a74d9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.