FDA label eb0f52ff-6461-402d-af73-71844b7d3841

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: 592cbe0f-e37d-436b-979f-5eeff4022dba
SPL ID: eb0f52ff-6461-402d-af73-71844b7d3841
Version: 6
Effective date: 2013-04-11
Source export date: 2026-10-12
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/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:29:17

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		eb0f52ff-6461-402d-af73-71844b7d3841	id
spl set id		592cbe0f-e37d-436b-979f-5eeff4022dba	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 WHEN USING THIS PRODUCT use only as directed do not bandage tightly or use with a heating paD avoid contact with eyes or mucous membranes do not apply to wounds or damaged skin STOP USE AND ASK A DOCTOR IF condition wors ens symptoms persist for more than 7 days or clear up and occur again within a few days redness is present irritation develops IF PREGNANT OR BREAST-FEEDING ask a health professional before use. KEEP OUT OF REACH OF CHILDREN In case of overdose, get medical 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.