Home FDA labels 6148c5e0-d631-4d8d-8972-123bedffff66 Antiperspirant Wipe for Women 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 Antiperspirant Wipe for Women
Generic name ALUMINUM CHLOROHYDRATE
Manufacturer FlawlessWipes, LLC
Product type HUMAN OTC DRUG
SPL set ID a94d0d85-2537-424f-87c8-6aeade047800
SPL ID 6148c5e0-d631-4d8d-8972-123bedffff66
Version 1
Effective date 2017-07-17
Source export date 2026-10-12
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/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:34:49 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 · 12 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 When using this product avoid contact with eyes. in case of eye contact, flush thoroughly with water. Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72 hours
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.