FDA.reportPublic FDA data

FDA label b3eed442-4346-6cd3-e053-2995a90a59dd

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
b3eed442-4345-6cd3-e053-2995a90a59dd
SPL ID
b3eed442-4346-6cd3-e053-2995a90a59dd
Version
1
Effective date
2020-11-12
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:28:08

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 use only as directed avoid contact with eyes do not apply to open wounds or damaged skin do not bandage tightly or use a heat pad Stop use and ask a doctor if condition worsens or if symptoms persist for more than 7 days irritation develops redness is present If pregnant or breast-feeding ask a health professional; before use Keep out of the reach of children If accidentally ingested, seek medical help or contact a Poison Control Center immediately, Replace cap firmly.

Reported adverse events (FAERS/openFDA)#

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