FDA label 32f37960-d0f2-4a9f-8fd0-53a6cb52c9dd

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: 3f26477b-3a60-49f2-a54f-ac2d80bac09d
SPL ID: 32f37960-d0f2-4a9f-8fd0-53a6cb52c9dd
Version: 2
Effective date: 2019-09-05
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:07:31

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		32f37960-d0f2-4a9f-8fd0-53a6cb52c9dd	id
spl set id		3f26477b-3a60-49f2-a54f-ac2d80bac09d	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. Stop using and see a doctor in case of suffering from any adverse side effects or skin irritation as follows while using this product. a. Red spots, edema, itchy sentations. etc., while using. b. In case of having above symptoms due to direct sunlight. 2. Do not use on spots affected bydermatitis and wounds. 3. Cautions for storage and use. a. After use, be sure to close the cap. b. Keep out of reach of children. c. Avoid prolinged exposure to extreme heat or cold and direct sunlight. *If disposable pouch product, use immediately after opening. *Do not apply in case of having severe allege reaction to wear sticking plaster or wet patch

Reported adverse events (FAERS/openFDA)#

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