FDA label 24d86c23-6655-00dc-e054-00144ff8d46c

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: 26911234-231b-4867-8fa6-3458a352a774
SPL ID: 24d86c23-6655-00dc-e054-00144ff8d46c
Version: 6
Effective date: 2015-11-18
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 06:30:56

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		24d86c23-6655-00dc-e054-00144ff8d46c	id
spl set id		26911234-231b-4867-8fa6-3458a352a774	set_id

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. •Avoid contact with eyes. •Stop use and ask a doctor if condition worsens, or symptoms last more than 7 days, or clear up and occur again within a few days. •Do not use on deep or puncture wounds, animal bites, or serious burns. •If pregnant or breast feeding, contact physician prior to use. • Do not use in large quantities, particularly over raw surfaces or blistered areas.

Reported adverse events (FAERS/openFDA)#

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