Home FDA labels 2901fddb-b514-1234-e063-6394a90a9208 Papatui Antiperspirant Deodorant Vanilla Shea 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 Papatui Antiperspirant Deodorant Vanilla Shea
Generic name ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Manufacturer PAPATUI LLC
Product type HUMAN OTC DRUG
SPL set ID 2901fddb-b513-1234-e063-6394a90a9208
SPL ID 2901fddb-b514-1234-e063-6394a90a9208
Version 1
Effective date 2024-12-11
Source export date 2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:09:10 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 Warnings For external use only. Do not use on broken skin. Stop use if rash or irritation occurs. Ask doctor before use if you have kidney disease. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.