DERLADIE LABORATOIRE PORE TIGHTENING AMPOULE

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
DERLADIE LABORATOIRE PORE TIGHTENING AMPOULE
Generic name
NIACINAMIDE
Manufacturer
LAON COMMERCE co ltd
Product type
HUMAN OTC DRUG
SPL set ID
0be5f72e-f80e-6cfa-e063-6394a90a3fc3
SPL ID
0be5f801-9960-dbac-e063-6394a90a86a1
Version
1
Effective date
2023-12-07
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:16:06
Harmonized routes table
Harmonized routes
TOPICAL

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

1. During using product or after use, if there are any abnormal symptoms or side effects such as red spots, swelling or itching in the area of use due to direct sunlight, consult with a specialist. 2. Refrain from using on areas with scars, etc. 3. Precautions for storage and handling A) Keep out of reach of chil dren B) Store away from direct sunlight 4. Since a high dose of niacinamide is prescribed, please adjust the amount after performing a skin sensitivity test when using for the first time

Reported adverse events (FAERS/openFDA)#

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