FDA label 7b4a996e-9504-ac06-e053-2991aa0a61d3

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: 4c3a0ff2-8c9c-5a83-e054-00144ff8d46c
SPL ID: 7b4a996e-9504-ac06-e053-2991aa0a61d3
Version: 2
Effective date: 2018-11-22
Source export date: 2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:13:05

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		7b4a996e-9504-ac06-e053-2991aa0a61d3	id
spl set id		4c3a0ff2-8c9c-5a83-e054-00144ff8d46c	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 In the use of the product if the following phenomenon happen, please stop using; if continue using the situation gets worse, please consult with the doctor 1) red, itchy, tingling 2) please stop using if any of the above symptoms appear because of the sun exposure 2 Wounds, eczema, skin inflammation in the face, please do not use 3 Storage precautions 1) seale immediately after using 2) please place in theplace where the infant are unable to access in case eating by mistake 3) avoid placing in high temperature, low temperature or direct sunlight field

Reported adverse events (FAERS/openFDA)#

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