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 2026-11-06
Source partition 4
Source file https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 06:58:09 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.