Home FDA labels 47e1c5f2-aa4b-ae7e-e063-6294a90abf33 Wipex 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)
Brand name Wipex
Generic name ANTIBACTERIAL WIPE
Manufacturer Unico International Trading Corporation
Product type HUMAN OTC DRUG
SPL set ID 144453a2-8335-77be-e063-6394a90ab676
SPL ID 47e1c5f2-aa4b-ae7e-e063-6294a90abf33
Version 6
Effective date 2026-01-08
Source export date 2026-09-28
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:18:57 Harmonized routes table Harmonized routes TOPICAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 13 matching rows.
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. Do not use in the eyes. In case of eye contact, rinse with water. If irritation develops, discontinue use. Consult a doctor if irritation continues for more than 72 hours. If swallowed seek medical attention or call a poison control center.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.