FDA label 083dc305-9c3c-4ccb-bd54-81cf4b3e3be6

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
3b75b7fb-62aa-4210-941f-b15589037141
SPL ID
083dc305-9c3c-4ccb-bd54-81cf4b3e3be6
Version
1
Effective date
2012-05-09
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:35:40

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: 1. For external use only. 2. Do not use on wounds or other infected areas. 3. Stop use if any of the following symptoms appear and consult a doctor if they persist. - Redness, swelling, itchiness, irritation, rash, etc. - Any of the above symptoms when exposed to direct sunlight. 4. Persists consult your doctor or pharmacist.

Reported adverse events (FAERS/openFDA)#

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