FDA.reportPublic FDA data

FDA label 479e730a-406a-49c8-adcc-8dfbca9d67f3

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
f280e942-30b1-4089-b4e5-53c36f4e2096
SPL ID
479e730a-406a-49c8-adcc-8dfbca9d67f3
Version
2
Effective date
2014-04-21
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:12:52

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

Warnings For external use only FLAMMABLE keep away from fire or flame, heat, sparks, and sources of static discharge When using this product avoid contact with eyes and mucous membranes if in eyes, rinse promptly and thoroughly with water discontinue use if irritation or redness develop Stop use and ask a doctor if irritation or redness occurs for more than 72 hours. 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.