FDA label 8caf9a28-d8f9-4df3-a8d2-d85034483c47

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: ad6f5eea-06b0-402f-bdc8-ab34168c2a72
SPL ID: 8caf9a28-d8f9-4df3-a8d2-d85034483c47
Version: 1
Effective date: 2018-07-06
Source export date: 2026-10-12
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:53:16

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		8caf9a28-d8f9-4df3-a8d2-d85034483c47	id
spl set id		ad6f5eea-06b0-402f-bdc8-ab34168c2a72	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 discontinue use if there are the following abnormalities. If you continue to use the product, the symptoms will worsen, so consult a dermatologist. ①In case of a red spot, swelling, itching, or irritation during use ②If there is any irritation after the application area is affected by sunlight. 2. Do not use on injured skin, eczema, and dermatitis in these areas. 3. Precautions during storage and handling ① Be sure to close the cap after using it. ② Keep Out of the reach of Children. ③Do not store in hot or cold place or in direct sunlight.

Reported adverse events (FAERS/openFDA)#

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