FOASU JIN MOISTURIZING ESSENCE

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 MOISTURIZING ESSENCE
Generic name: NIACINAMIDE, ADENOSINE
Manufacturer: HANSCOS Co.,Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: d8f9c89e-dbae-3967-e053-2a95a90a7363
SPL ID: d8f9ca3e-74f8-e5d5-e053-2995a90a0b81
Version: 1
Effective date: 2022-02-26
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:10:00

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 MOISTURIZING ESSENCE	openfda.brand_name
generic name		NIACINAMIDE, ADENOSINE	openfda.generic_name
manufacturer name		HANSCOS Co.,Ltd.	openfda.manufacturer_name
ndc	package	77964-003-01	openfda.package_ndc
ndc	product	77964-003	openfda.product_ndc
ndc11	package	77964000301	derived:openfda.package_ndc
spl id		d8f9ca3e-74f8-e5d5-e053-2995a90a0b81	id
spl set id		d8f9c89e-dbae-3967-e053-2a95a90a7363	set_id
unii		25X51I8RD4	openfda.unii
unii		K72T3FS567	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.