FDA label 0d23c82b-f442-4b2e-be7f-5ebf62c5cdd6

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
33c2b585-fc7e-4ca5-8f88-49e745389951
SPL ID
0d23c82b-f442-4b2e-be7f-5ebf62c5cdd6
Version
3
Effective date
2020-07-17
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:43:03

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 ■ Keep out of eyes, ears, or mouth. ■ In case of eye contact, flush eyes thoroughly with water. ■ Avoid contact with broken skin. ■ Do not inhale or ingest. Stop use and ask a doctor if ■ Redness or irritation develop. ■ Condition persists for more than 72 hours. Keep out of reach of children. ■ Children should be supervised by an adult when using this product. ■ 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.