FDA label f65d52ae-8348-4691-b432-7ca05fad5fd3

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: 7bf21905-975a-472d-a2d6-a9c1408e7f95
SPL ID: f65d52ae-8348-4691-b432-7ca05fad5fd3
Version: 2
Effective date: 2016-11-18
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 01:50:49

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		f65d52ae-8348-4691-b432-7ca05fad5fd3	id
spl set id		7bf21905-975a-472d-a2d6-a9c1408e7f95	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 the external use only. When using this product use as directed. Do not bandage tightly or use with heating pad. Avoid contact with eyes and mucous membranes. Do not apply to wounds or damaged, broken, or irritated skin. If severe burning sensation occurs, discontinue use immediately. Do not expose the area treated with product to heat or direct sunlight. Stop use and ask a doctor if conditions worsen, redness is present, irritation develops. If swallowed, get medical help or contact a Poison Control Center right away. IF MEDICINE COMES IN CONTACT WITH HANDS, WASH WITH SOAP AND WATER.

Reported adverse events (FAERS/openFDA)#

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