FDA label 0e9551ee-2843-451b-9c48-5cebdfcb75c8

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
e626d2cc-caf8-4515-9959-d2def58c7be3
SPL ID
0e9551ee-2843-451b-9c48-5cebdfcb75c8
Version
1
Effective date
2010-09-27
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 06:00:00

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

For external use only Do not use on wounds or damaged skin with heating pads or heating devices with other ointments, creams, sprays or liniments with tight bandages When using this product avoid contact with eyes Stop use and ask a doctor if: a rash appears condition worsens or if symptoms persist for more than 7 days, or clear up and occur again within a few days If pregnant or breast-feeding, ask a doctor before use.

Reported adverse events (FAERS/openFDA)#

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