FDA label c2e80852-3bb9-41c7-a83b-e341ba01c8f7

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
fe16d57b-469e-4158-b719-80fd18d9d858
SPL ID
c2e80852-3bb9-41c7-a83b-e341ba01c8f7
Version
1
Effective date
2020-08-06
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:34:30

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.