FOASU JIN POWDERWASH

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: FOASU JIN POWDERWASH
Generic name: ALLANTOIN, PANTHENOL
Manufacturer: HANSCOS Co.,Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: d8fa5b99-b9aa-fb14-e053-2a95a90a74d9
SPL ID: d8fa5b99-b9ab-fb14-e053-2a95a90a74d9
Version: 1
Effective date: 2022-02-27
Source export date: 2026-10-30
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/8d15bdc5962e7531569eaeb5b1b2e4919574d40a6782ab67345a27b890175a00/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:54:13

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		FOASU JIN POWDERWASH	openfda.brand_name
generic name		ALLANTOIN, PANTHENOL	openfda.generic_name
manufacturer name		HANSCOS Co.,Ltd.	openfda.manufacturer_name
ndc	package	77964-005-01	openfda.package_ndc
ndc	product	77964-005	openfda.product_ndc
ndc11	package	77964000501	derived:openfda.package_ndc
spl id		d8fa5b99-b9ab-fb14-e053-2a95a90a74d9	id
spl set id		d8fa5b99-b9aa-fb14-e053-2a95a90a74d9	set_id
unii		WV9CM0O67Z	openfda.unii
unii		344S277G0Z	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

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.

Reported adverse events (FAERS/openFDA)#

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