FDA.reportPublic FDA data

FDA label 19d9e022-e93e-4e48-8b80-a5151a1f51e8

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
8a8e7cef-01f6-44c1-9de8-1071f9cd0f57
SPL ID
19d9e022-e93e-4e48-8b80-a5151a1f51e8
Version
6
Effective date
2018-03-08
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:33:35

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. This package is intended for institutional use only. Do not use in the eyes, over large areas of the body or if you are allergic to any of the ingredients. Ask a doctor before use in case of deep or puncture wounds, animal bites or serious burns. When using this product do not use longer than 1 week unless directed by a doctor. Stop use and ask a doctor if the condition persists or gets worse or if a rash or other allergic reaction develops.

Reported adverse events (FAERS/openFDA)#

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