FDA.reportPublic FDA data

FDA label af21fa15-71ed-4744-b84c-b678caa4d3fe

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
de712d51-d2f8-4a31-b0a6-e6c8f599946b
SPL ID
af21fa15-71ed-4744-b84c-b678caa4d3fe
Version
2
Effective date
2018-07-11
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 05:22:57

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 For external use only. When using this product • avoid contact with the eyes or mucous membranes • do not apply to wounds or damaged skin • do not apply to the irritated skin or if excessive irritation develops • do not bandage • do not use with heating pad or device Stop use and ask a doctor if • condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days. If pregnant or breastfeeding ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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