FDA label 7aeb66f4-9262-41cd-a2ac-e9f19c8011d6

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: d0982c95-51a1-4110-85c7-9100002e238f
SPL ID: 7aeb66f4-9262-41cd-a2ac-e9f19c8011d6
Version: 2
Effective date: 2022-02-16
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:52:38

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		7aeb66f4-9262-41cd-a2ac-e9f19c8011d6	id
spl set id		d0982c95-51a1-4110-85c7-9100002e238f	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 1. Consult a specialist if you have abnormal symptoms or side effects such as red spots, swelling, or itching in the area of use due to direct sunlight during or after using cosmetics. 2. Do not use this product in areas with scratches, eczema, or dermatitis. 3. Storage and Handling Precautions 1) Always close the cap after use. 2) Please keep out of reach of infants and children. 3) Please keep it away from direct sunlight. 4. If an infant or a child takes cosmetics accidently, consult a medical doctor immediately and take emergency measures. 5. Do not use it for infants under the age of three.

Reported adverse events (FAERS/openFDA)#

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