FDA label 07575a7d-b468-7abc-e063-6294a90ab0fd

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
f1fd64d3-8f8f-4814-a9e6-f1cd166748d3
SPL ID
07575a7d-b468-7abc-e063-6294a90ab0fd
Version
4
Effective date
2023-10-10
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 06:34:47

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 ​DO NOT USE if pregnant or breast-feeding. For external use only When using this product use only as directed do not get into the eyes or mucous membranes do not apply to wounds or damaged skin do not bandage tightly Stop use and ask a doctor if: Excessive irritation develops Pain worsens or does not improve within 7 days or clears up and appears again in a few days.

Reported adverse events (FAERS/openFDA)#

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