FDA label c6e6e4ca-5c8f-494f-9499-e791571b82de

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
c5120583-0f3a-40c4-a20d-155d12044e7d
SPL ID
c6e6e4ca-5c8f-494f-9499-e791571b82de
Version
1
Effective date
2010-07-08
Source export date
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:10:34

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 awayImmediately.

Reported adverse events (FAERS/openFDA)#

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