FDA.reportPublic FDA data

FDA label 9aa3fea7-6aa9-6926-e053-2a95a90a582e

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
c7edd665-e5a1-4c79-82c3-4e2d325882c4
SPL ID
9aa3fea7-6aa9-6926-e053-2a95a90a582e
Version
2
Effective date
2019-12-26
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:40:18

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 ​ apply to wounds or damaged skin apply over large areas of the body ​When using this product ​ avoid contact with eyes or mucous membrandes ​Stop use and ask a doctor if ​symptoms persist for more than 7 days or clear up and occur again within a few days rash develops ​If pregnant or breast feeding, ​ consult a health professional before use. ​Keep out of reach of children. ​ If swallowed, get metical 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.