FDA label e764775a-86b6-4805-9f6b-9321be31957c

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: f1ab739d-bad5-49f2-8c0a-7688aef64d9b
SPL ID: e764775a-86b6-4805-9f6b-9321be31957c
Version: 5
Effective date: 2022-11-22
Source export date: 2026-10-12
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:26:33

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		e764775a-86b6-4805-9f6b-9321be31957c	id
spl set id		f1ab739d-bad5-49f2-8c0a-7688aef64d9b	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 getting into the eyes or on mucous membranes. Do not apply to irritated skin and discontinue use if excessive irritation develops. If pain persists for more than 7 days, or redness is present, or in conditions affecting children under 12 years of age consult a physician immediately. Do not expose treated area to heat or direct sunlight. Do not bandage. Do not apply to wounds or damaged skin. As with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using this product.

Reported adverse events (FAERS/openFDA)#

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