FDA.reportPublic FDA data

FDA label ea25800d-87f4-4545-a28d-b9138f8b115e

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
e798ab66-d0a7-4b60-961e-e833e2e33a18
SPL ID
ea25800d-87f4-4545-a28d-b9138f8b115e
Version
1
Effective date
2012-02-06
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:21:15

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: If side-effects, such as redness, itching or swelling occur, discontinue use. If airritation continues after discontinuing use, consult a dermatologist. 1. If a red area develops using this product or there is swelling or itchyness, consult a dermatologist. 2. Exposure to direct sunlight may cause side-effects as above. 3. Do not apply product to an area of skin that is affected by eczema or dermatitis. 4. Wash eyes immediately and thoroughly if product enters eyes.

Reported adverse events (FAERS/openFDA)#

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