FDA label 09696541-d750-4d1d-b6d9-e7f6edae9261

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)

SPL set ID: b1634462-bdda-4a2f-b54a-c3eba33ed700
SPL ID: 09696541-d750-4d1d-b6d9-e7f6edae9261
Version: 2
Effective date: 2021-10-20
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:22:20

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 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		09696541-d750-4d1d-b6d9-e7f6edae9261	id
spl set id		b1634462-bdda-4a2f-b54a-c3eba33ed700	set_id

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 Warnings: 1. When using it for the first time, you can feel a light irritation but it’s rather close to a refreshed feeling not pain. Sometimes, sensitive skin type may feel itching but it will not last more than a few minutes. 2. When using or after using Micro-needle Patch, if you have abnormal symptoms such as red spot, swelling or itching or any side effects by direct sunlight, please consult with a specialist. 3. Do not use in areas with scratches. 4. Safety and storage precautions. A) Keep out of children’s reach B) Keep away from direct sunlight C) Use immediately after opening

Reported adverse events (FAERS/openFDA)#

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