FDA label 9b1ade7e-a9df-46c0-a84f-9be8bef189ec

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: 100c83d5-6c58-4629-8204-a63fe5872628
SPL ID: 9b1ade7e-a9df-46c0-a84f-9be8bef189ec
Version: 2
Effective date: 2011-08-02
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:58:40

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		9b1ade7e-a9df-46c0-a84f-9be8bef189ec	id
spl set id		100c83d5-6c58-4629-8204-a63fe5872628	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 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 in the case of a deep puncture wound, animal bites or serious burns Stop use and ask a doctor if - the condition persists or gets worse - a rash or other allergic reaction develops - symptoms last for more than 7 days or clear up and come back within a few days Keep out of reach of children. If swallowed, 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.