FDA label acc165fb-a26e-4db6-99d1-b22b776ed04f

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: 1b312e93-dd06-4e72-ac6c-5283405da417
SPL ID: acc165fb-a26e-4db6-99d1-b22b776ed04f
Version: 1
Effective date: 2010-12-14
Source export date: 2026-10-12
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/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:52:16

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		acc165fb-a26e-4db6-99d1-b22b776ed04f	id
spl set id		1b312e93-dd06-4e72-ac6c-5283405da417	set_id

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

WARNING: Discontinue use if skin irritation develops or increases. If irritation persists, consult a health care practitioner.

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