FDA label f4ee870c-a1de-1d42-e053-2a95a90ada2d

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
142c6ff2-71cd-0f4e-e054-00144ff88e88
SPL ID
f4ee870c-a1de-1d42-e053-2a95a90ada2d
Version
4
Effective date
2023-02-17
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 05:24:45

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

For external use only. When using this product use only as directed avoid contact with eyes and mucous membranes do not apply to wounds, damaged or irritated skin do not bandage or cover with wrap or use heating pad do not use 1 hour prior to bathing or 30 minutes after bathing Stop use and ask a doctor if condition worsens severe skin irritation occurs pain persists for more than 7 days pain clears up and then reocurs a few days later. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center immediately If pregnant or breast-feeding ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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