FDA label 825570e7-df39-24ec-e053-2a91aa0ab07e

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
ea36aec1-0053-492a-b931-fff89eb687c3
SPL ID
825570e7-df39-24ec-e053-2a91aa0ab07e
Version
2
Effective date
2019-02-20
Source export date
2026-09-28
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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:13

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

Reported adverse events (FAERS/openFDA)#

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