FDA.reportPublic FDA data

Antiperspirant Wipe

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
Generic name
ALUMINUM CHLOROHYDRATE
Manufacturer
Stock Your Home
Product type
HUMAN OTC DRUG
SPL set ID
326c944a-8beb-d33d-e063-6294a90ae2a9
SPL ID
584dffd9-059e-ee73-e063-6394a90ad62d
Version
3
Effective date
2026-08-05
Source export date
2026-08-08
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-08/13477f292fde418ab8b889dedaeed5fd633628cccdf0fe6d78a20f4b857aa1ee/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
b39f3b00ad50d2e1b32aaf429248c6081e8799b35bce715b4fccb8cfa1ac4546
Import run
20260810T161303Z
Imported at
2026-08-10 17:34:50
Harmonized routes table
Harmonized routes
TOPICAL

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 ■ on broken or irritation skin ■ immediately after shaving Ask a doctor before use if you have kidney disease When using this product ■ do not use in or near eyes ■ apply to underarms only Stop use and ask a doctor if rash or irritation develops