FDA.reportPublic FDA data

FDA label 22a4c65f-a7a3-4be7-812b-12c81ea4c6f9

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
b14e4b20-0bcb-4252-ba2d-1d07c73632f0
SPL ID
22a4c65f-a7a3-4be7-812b-12c81ea4c6f9
Version
1
Effective date
2016-10-11
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:26

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 Warnings: 1. If following symptoms develop, continuing use of the product might aggravate the symptoms, thus discontinue use and consult a doctor. 1)Red spots, swelling, itching or dermatitis. 2)Above symptoms on the applied area after exposure to direct sunlight. 2. Avoid contact for areas with wounds, eczema or dermatitis. 3.Caution for storage and handling 1) Be sure to put the cap on after use. 2) keep out of reach of children. 3) Keep out of high temperature, low temperature or direct sunlight.

Reported adverse events (FAERS/openFDA)#

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