FDA.reportPublic FDA data

FDA label c5dc9c7b-d114-4e0a-ad3b-2ba289092828

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
1fc313f6-01ae-49d9-b46f-b7baa0e21e23
SPL ID
c5dc9c7b-d114-4e0a-ad3b-2ba289092828
Version
3
Effective date
2021-11-29
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:39

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. Please consult with a physician or other qualified health provider if you have abnormal symptoms such as red spot, swelling or itching, or side effects caused by exposure to direct sunlight, during or after use of the product. 2. Avoid areas with wounds or other sensitive areas. 3. Don’t spray this product around eyes and mucous membrane! 4. Precautions for storage and handling. 1)Keep out of reach of children. 2)Avoid direct exposure to sunlight.

Reported adverse events (FAERS/openFDA)#

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