FDA label 98d2918a-a82e-2dfb-e053-2995a90a5d6c

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
433d86c2-c2cc-07fd-e054-00144ff88e88
SPL ID
98d2918a-a82e-2dfb-e053-2995a90a5d6c
Version
3
Effective date
2019-12-03
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 05:59:07

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 For external use only. Do not use on wounds or damaged skin or if you are allergic to ingredients in the product. When using this product avoid contact with eyes. If product gets into eyes, rinse thoroughly with water. do not bandage tightly or use a heating pad. Stop use and ask a doctor if rash appears. condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and occur again within a few days. If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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