FDA label a0c8c7f1-deb4-45ac-915b-6cb00218222a

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: 88242e28-6470-4048-9fa3-44202e1a9018
SPL ID: a0c8c7f1-deb4-45ac-915b-6cb00218222a
Version: 2
Effective date: 2022-08-10
Source export date: 2026-10-12
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:40:55

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		a0c8c7f1-deb4-45ac-915b-6cb00218222a	id
spl set id		88242e28-6470-4048-9fa3-44202e1a9018	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 ■ If you experience any symptoms such as redness, swelling or itchiness during usage or from exposure to direct sunlight after usage, suspend use and consult a physician ■ Do not use on wounds or other areas of skin irritation ■ Keep out of reach of children ■ Store away from direct sunlight

Reported adverse events (FAERS/openFDA)#

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