FDA.reportPublic FDA data

FDA label 416d76ab-d53a-401e-a2e2-1dce3a870cbd

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
043dcb7d-c2fa-4111-bd4d-dba21b7469db
SPL ID
416d76ab-d53a-401e-a2e2-1dce3a870cbd
Version
1
Effective date
2018-07-06
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 07:49:11

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 area 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.