FDA label 1baf2152-0ac0-64cc-e063-6394a90aa527

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: ec6e9a5b-c61f-a385-e053-2995a90ac936
SPL ID: 1baf2152-0ac0-64cc-e063-6394a90aa527
Version: 3
Effective date: 2024-06-24
Source export date: 2026-09-28
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:12:39

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		1baf2152-0ac0-64cc-e063-6394a90aa527	id
spl set id		ec6e9a5b-c61f-a385-e053-2995a90ac936	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

1. During the application of this product, if abnormal symptoms or side effects occur, such as erythema, redness, swelling or itching due to direct light, please seek for medical advice and consult a professional doctor immediately. 2. Avoid using it directly on the wounded parts. 3. Keep the product out of reach of children. 4. If it accidentally gets into the eyes, immediately wash and flush eyes with clean water. 5. This product may cause skin and body allergies or aggravate existing abnormal skin reactions (edema, inflammation, etc.). If you have experienced prior allergic reactions,consult a professional doctor or pharmacist before use.

Reported adverse events (FAERS/openFDA)#

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