DERMAHAN THE WHITENING MOISTURIZING MASK

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
DERMAHAN THE WHITENING MOISTURIZING MASK
Generic name
NIACINAMIDE, ADENOSINE
Manufacturer
LAON COMMERCE co ltd
Product type
HUMAN OTC DRUG
SPL set ID
cf131624-b223-55c0-e053-2995a90a31f3
SPL ID
cf131624-b222-55c0-e053-2995a90a31f3
Version
1
Effective date
2021-10-24
Source export date
2026-10-30
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/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:24:40
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

■ if following abnormal symptoms persist, discontinue use Irritation around the eyes, ears, mucous membranes, including the mouth, under the skin irritation and rashes ■ Stop immediately and consult a doctor if you experience 1) Hypersensitivity symptoms such as erythema, itching and dermatitis. 2) Skin Irritation 3) Following Instructions when using medication (1) For external use only (Do not use internally) (2) Avoid getting into the eyes (if contact occurs, wash well with clean water)

Reported adverse events (FAERS/openFDA)#

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