FDA label 531cc62e-fb0e-458e-93d8-e17324d2727f

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
ab8b4903-9d1a-4f5d-aa6b-ae96c5542edf
SPL ID
531cc62e-fb0e-458e-93d8-e17324d2727f
Version
3
Effective date
2013-03-26
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 05:17:03

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 on children under two years of age except under the advice and supervision of a doctor. stop use and ask a doctor if irritation occurs, if condition worsens, or there is not improvement within four weeks. for externam use only avoid contact with eyes, scalp, vagina, penis, scortum and anus do not ingest do not use on open wounds in case of accidental ingestion, contacgt a physician, emergency medical do not use if you are know to be sensitive to any of the ingredients in this product

Reported adverse events (FAERS/openFDA)#

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