FDA label 263a2220-9939-e363-e063-6394a90a23c5

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
263a2220-9938-e363-e063-6394a90a23c5
SPL ID
263a2220-9939-e363-e063-6394a90a23c5
Version
1
Effective date
2024-11-06
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:04:52

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

Warning 1). For external use only, use with caution when the skin has wounds.swelling. or pus; 2). Store in a cool dry place, avoid direct sunlight 3). lf you feel unwell during use, please stop using it immediately. 4).Use according to the instructions; 5). prevent children from swallowing by mistake; 6). This product may cause allergic reactions to a small number ofpeople, please stop using it immediately if you feel unwell. Beforeeach use, please select a small piece of skin for an allergy test There isno adverse skin reaction 24 hours before using this product 7). Avoid contact with eyes, lf this product accidentally enters theeyes, please rinse with plenty of water and seek medical attentionimmediately.

Reported adverse events (FAERS/openFDA)#

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