FDA.reportPublic FDA data

FDA label d5477640-4af0-5ebe-e053-2995a90a6e7e

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
6279eef3-7688-bedd-e053-2991aa0ad9b1
SPL ID
d5477640-4af0-5ebe-e053-2995a90a6e7e
Version
2
Effective date
2022-01-10
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 05:23:24

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. Please stop using the product for the following symptoms and it is advised to consult a dermatologist when it gets worse. a)Red dots, swelling, itching or irritation while using the product. b)Above symptoms at direct sunlight. 2. Please do not apply on the wounded, eczema or inflammation area. 3. Storage & Handling a)Please keep away from infants and little children, b)Please do not keep at extremely high or low temperature or under direct sunlight. 4. Please avoid using around eye circles.

Reported adverse events (FAERS/openFDA)#

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