FDA.reportPublic FDA data

Papatui Antiperspirant Deodorant Lush Coconut

Manufacturer
PAPATUI LLC
Effective date
2024-12-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:42:12

Label at a glance#

ProductPapatui Antiperspirant Deodorant Lush Coconut
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure10 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION

PAPATUI™

48-Hour Antiperspirant Deodorant

Antitranspirant 48H

48-HOUR SWEAT & ODOR PROTECTION ->

INVISIBLE LONG-LASTING FRESHNESS ->

PARABEN FREE -> PHTHALATE FREE ->

CRUELTY FREE -> VEGAN

LUSH COCONUT

2.6 oz/73 g

OTC - ACTIVE INGREDIENT SECTION

Drug Facts

Active Ingredients

Aluminum Zirconium Trichlorohydrex Gly 16%

OTC - PURPOSE SECTION

Purpose

Antiperspirant

INDICATIONS & USAGE SECTION

Uses

Reduces underarm wetness.

WARNINGS SECTION

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.

DOSAGE & ADMINISTRATION SECTION

For external use only

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

RECENT MAJOR CHANGES SECTION

Uses

Reduces underarm wetness.

INSTRUCTIONS FOR USE SECTION

Directions

Apply to clean, dry underarms only.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Dimethicone, Stearyl Alcohol, C15-19 Alkane, Diheptyl Succinate, C12-15 Alkyl Benzoate, Water, Hydrogenated Castor Oil, Cetyl Alcohol, Silica, Aluminum Starch Octenylsuccinate, Fragrance, Capryloyl Glycerin/Sebacic Acid Copolymer, Balanites Aegyptiaca Kernal Oil, Myristyl Alcohol, Tocopheryl Acetate, Coumarin, Limonene, Linalool.

OTC - QUESTIONS SECTION

Questions?

Call toll-free 1-844-4PAPATUI, Mon-Fri

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lush Coconut PDPLush Coconut PDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83850-102-73Papatui Antiperspirant Deodorant Lush Coconut73 g in 1 CANISTERSTICK733

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83850-102PAPATUI ANTIPERSPIRANT DEODORANT LUSH COCONUT (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY) STICK [PAPATUI LLC]3Current NDC, 1 package rows20241213_0be47495-6a89-9625-e063-6394a90ae09c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83850-10283850-102-73

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
LINALOOL, (+)-F4VNO44C09IACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB
STEARYL ALCOHOL2KR89I4H1YIACT
CETYL ALCOHOL936JST6JCNIACT
DIMETHICONE92RU3N3Y1OIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
LIMONENE, (+)-GFD7C86Q1WIACT
C15-19 ALKANECI87N1IM01IACT
BALANITES AEGYPTIACA SEED OIL75T177G59EIACT
COUMARINA4VZ22K1WTIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)N7YC58165TIACT
DIHEPTYL SUCCINATE057N7SS26YIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
MYRISTYL ALCOHOLV42034O9PUIACT
WATER059QF0KO0RIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Papatui Antiperspirant Deodorant Lush CoconutALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYPAPATUI LLC0be47495-6a89-9625-e063-6394a90ae09c2024-12-11WarningsExact identifier
ndc (package): 83850-102-73
ndc (product): 83850-102
ndc11 (package): 83850010273
spl id: 2901f5cc-ab22-e3f1-e063-6394a90a4c6d
spl set id: 0be47495-6a89-9625-e063-6394a90ae09c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.