FDA label cbe6d2d9-0307-4dd4-8a0c-ab6bca9f7477

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: cfa5b5a7-7900-40c7-94e3-3326db305e0e
SPL ID: cbe6d2d9-0307-4dd4-8a0c-ab6bca9f7477
Version: 1
Effective date: 2015-09-15
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:16:38

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		cbe6d2d9-0307-4dd4-8a0c-ab6bca9f7477	id
spl set id		cfa5b5a7-7900-40c7-94e3-3326db305e0e	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 Warnings: 1. Please stop using when you have trouble as below. Consult to dermatologists when it gets worse. A, skin has red spot, swollen or itchiness and sensational skin B. Skin has those symptoms by direct sunlight. 2. Do not use wounds, eczema, dermatitis 3. Precautions A. Must keep closing lid after using. B. Keep out of children C. Do not keep in high or low temperatures and avoid direct sunlight 4. Similar products with same components (More than 2% of arbutin) are reported in “Human applicable test data” as an example of papule and mild itching.

Reported adverse events (FAERS/openFDA)#

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