Home FDA labels 47e5f195-d2d1-cacd-e063-6394a90a2adf Roll On Anti-Perspirant Deodorant 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 Roll On Anti-Perspirant Deodorant
Generic name ALUMINUM CHLOROHYDRATE
Manufacturer Keefe Group
Product type HUMAN OTC DRUG
SPL set ID 9a1bd5aa-8720-42fe-a157-d06d122a893c
SPL ID 47e5f195-d2d1-cacd-e063-6394a90a2adf
Version 14
Effective date 2026-01-08
Source export date 2026-09-28
Source partition 13
Source file https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:38:48 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 · 10 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. Keep out of reach of children. Do not use on broken skin. Stop use if rash or irritation occurs. Ask a doctor before use if you have kidney disease. If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.