FDA label 1c55c2b5-4a85-0204-e063-6394a90a2231

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
2cf3e7df-935b-4083-a732-504a421b8284
SPL ID
1c55c2b5-4a85-0204-e063-6394a90a2231
Version
3
Effective date
2024-07-03
Source export date
2026-10-12
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/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:07:54

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 Flammable. Keep away from heat or flame. Do not eat. Discard after single use. -------------------------------------------------------------------------------------------------------- When using this product ■ do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. ■ avoid contact with brocken skin or on mucous membranes. ■ do not inhale or ingest. ■ do not reuse. there is a risk of infection from reusing the pad. -------------------------------------------------------------------------------------------------------- Stop use and ask a doctor if irritation or rash appears and lasts.

Reported adverse events (FAERS/openFDA)#

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