FDA label 5a971a0a-f997-dee0-e063-6394a90a12df

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
5fbc4665-d9cb-4785-b066-4f74a4bdec9a
SPL ID
5a971a0a-f997-dee0-e063-6394a90a12df
Version
6
Effective date
2026-09-03
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:00:55

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. Flammable, keep away from fire or flame. Do not use • with electrocautery procedures • longer than 1 week unless directed by a doctor When using this product • do not get into eyes • do not apply over large areas of the body • in case of deep or puncture wounds, animal bites or serious burns, consult a doctor Stop use and ask a doctor if • irritation and redness develop • condition gets worse or persists for more than 72 hours Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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