FDA.reportPublic FDA data

FDA label 147963c6-4b97-8520-e063-6394a90aab7f

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
0d6d4200-583b-3fda-e063-6394a90aac3f
SPL ID
147963c6-4b97-8520-e063-6394a90aab7f
Version
2
Effective date
2024-03-25
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:12:46

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 · Keep out of reach of children and pets. · Dispose of product thoroughly. · Do not flush down the toilet. · Keep away from eyes. In case of contact with eyes, rinse immediately with plenty of water for several minutes. · Do not ingest. In case of ingestion, do not induce vomiting and consult a doctor immediately. · If you have hypersensitivity to any of the components of the formula, do not use the product. · Stop usage if skin irritation occurs and consult a doctor, keep wipes inside the original packaging.

Reported adverse events (FAERS/openFDA)#

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