FDA.reportPublic FDA data

FDA label 1b1c1704-ed40-5cbf-e063-6294a90a219a

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
0fe60023-c917-7b9a-e063-6294a90a9d2d
SPL ID
1b1c1704-ed40-5cbf-e063-6294a90a219a
Version
4
Effective date
2024-06-17
Source export date
2026-11-06
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:45:09

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 Ask a doctor before use if you have ■deep or puncture wounds ■animal bites ■serious burns When using this product ■do not use in or near the eyes ■do not apply over large areas of the body or in large quantities ■do not apply over raw surfaces or blistered areas. Stop use and ask a doctor if ■condition worsens ■symptoms persist for more than 7 days, or clear up and occur again within a few days. Keep out of reach of children. If 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.