FDA label 37d4cc31-7bb1-4d5c-b8b1-832d1a569d2f

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: c3f2c30b-e222-4772-9016-886051200934
SPL ID: 37d4cc31-7bb1-4d5c-b8b1-832d1a569d2f
Version: 2
Effective date: 2012-04-17
Source export date: 2026-10-12
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/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:03:13

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		37d4cc31-7bb1-4d5c-b8b1-832d1a569d2f	id
spl set id		c3f2c30b-e222-4772-9016-886051200934	set_id

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

Warnings sections page 1 of 1 · 1 matching rows.

Warnings For External Use Only Stope use and ask doctor if irritation or redness develops.

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