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 2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:30:54 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.