FDA.reportPublic FDA data

FDA label 0dbc1594-d0ff-4e73-b1bb-81b49221f892

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
50b65dab-e5b5-42b1-a1a3-719bf070b0ba
SPL ID
0dbc1594-d0ff-4e73-b1bb-81b49221f892
Version
2
Effective date
2018-01-31
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 06:03:01

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. Avoid contact with eyes. Flammable: Do not use while smoking or near heat or flame. Do not use in large quantities, particularly over raw surfaces or blistered areas, on large areas of the body or on a cut, irritated or swollen skin, or for more than one week without consulting a physician. Stop use and ask a doctor if: conditions worsen, symptoms persist for more than 7 days or clear up and occur again within a few days. If pregnant or breast feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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