FDA label 56973c43-9d51-e3a0-e063-6294a90a7835

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
560ba2ca-ad0f-9202-e063-6294a90aaefd
SPL ID
56973c43-9d51-e3a0-e063-6294a90a7835
Version
3
Effective date
2026-07-14
Source export date
2026-11-06
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:49:46

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

For external use only Do not use: in the eyes if you are allergic to any of the ingredients over large areas of the body longer than 1 week unless directed by a doctor Ask a doctor before use if you have: animal bites serious burns deep or puncture wounds Stop use and ask a doctor if condition persists or gets worse rash or other allergic reaction develops

Reported adverse events (FAERS/openFDA)#

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