FDA label 1f49d242-3d5c-4ed8-afe4-283b8dbcfc21

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
778f0939-2597-45ae-b0d0-aeeead6c2102
SPL ID
1f49d242-3d5c-4ed8-afe4-283b8dbcfc21
Version
1
Effective date
2020-08-11
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:50:51

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: hands -------------------------------------------------------------------------------------------------------- Flammable. Keep away from fire or flame -------------------------------------------------------------------------------------------------------- When using this product ㆍkeep out of eyes. In case of contact with eyes, flush thoroughly with water. ㆍavoid contact with broken skin ㆍdo not inhale or ingest -------------------------------------------------------------------------------------------------------- Stop use and ask a doctor if ㆍirritation or redness develops ㆍcondition persists for more than 72 hours

Reported adverse events (FAERS/openFDA)#

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