FDA label 22963d1f-6027-41bc-af47-e998fd7c0c0c

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: 773895fb-cebd-431f-a7bc-fdd72f93df6e
SPL ID: 22963d1f-6027-41bc-af47-e998fd7c0c0c
Version: 1
Effective date: 2013-07-29
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 01:26:01

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		22963d1f-6027-41bc-af47-e998fd7c0c0c	id
spl set id		773895fb-cebd-431f-a7bc-fdd72f93df6e	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

- stop using the product and consult with a dermatologist or gynecologist if any of the following signs or symptoms appears rash, swelling, itching and irritation during its use in case any sign or symptom above appears on the applied area with the direct sunlight - do not use in the area, such as, of wound, eczema and dermatitis

Reported adverse events (FAERS/openFDA)#

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