FDA label 91de239c-de3a-2c62-e053-2a95a90a3163

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
91de4235-5919-626d-e053-2995a90a8cb0
SPL ID
91de239c-de3a-2c62-e053-2a95a90a3163
Version
1
Effective date
2019-09-06
Source export date
2026-11-06
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:40:59

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.