FDA label cde18d5d-2539-415c-8832-021bb4390227

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: 4472cd16-82be-4e54-a489-039d9f3c4332
SPL ID: cde18d5d-2539-415c-8832-021bb4390227
Version: 1
Effective date: 2014-03-02
Source export date: 2026-10-12
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:33:55

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		cde18d5d-2539-415c-8832-021bb4390227	id
spl set id		4472cd16-82be-4e54-a489-039d9f3c4332	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

A. Please stop using the product in anyone of the following cases: 1) Rash, swelling, itching, irritation, and other abnormal reactions on the skin after using the product. 2) When the abnormalities above appear on the skin due to direct sunlight, etc. B. Do NOT use on a scar, or skin affected by dermatitis, eczema, etc. C. Notes for Storage 1) Make sure to close the lid after use. 2) Keep away from babies and children. 3) Do not store in high/low temperature or under direct sun light. Abnormal products will be compensated for according to “Standard for Consumer Dispute Resolution” by Fair Trade Commission

Reported adverse events (FAERS/openFDA)#

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