FDA label 371652a2-8b3f-4a42-934f-7b9a2565d51c

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
69aeb7c8-9ee6-4b81-91c0-3472f33a5344
SPL ID
371652a2-8b3f-4a42-934f-7b9a2565d51c
Version
1
Effective date
2018-07-10
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:42:23

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.