PAPATUI ANTIPERSPIRANT DEODORANT SANDALWOOD SUEDE- aluminum zirconium trichlorohydrex gly stick

Papatui Antiperspirant Deodorant Sandalwood Suede by

Drug Labeling and Warnings

Papatui Antiperspirant Deodorant Sandalwood Suede by is a Otc medication manufactured, distributed, or labeled by Forward 7, KDC/One Development Corporation, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DESCRIPTION

PAPATUI™

48-HOUR ANTIPERSPIRANT DEODORANT

ANTITRANSPIRANT 48H

48-HOUR SWEAT & ODOR PROTECTION ->

INVISIBLE LONG-LASTING FRESHNESS ->

PARABEN FREE -> PHTHALATE FREE ->

CRUELTY FREE -> VEGAN

Sandalwood Suede

2.6 oz/ 73 g

ACTIVE INGREDIENT

Drug Facts

Active Ingredients

Aluminum Zirconium Trichlorohydrex Gly 16%

PURPOSE

Purpose

Antiperspirant

INDICATIONS & USAGE

Uses

Reduces underarm wetness.

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.

For external use only.

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

INSTRUCTIONS FOR USE

Directions

Apply to clean, dry underarms only.

INACTIVE INGREDIENT

INACTIVE INGREDIENT

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, Citronellol, Coumarin, Limonene, Linalool.

QUESTIONS

Questions? Call toll-free 1-844-4PAPATUI, Mon-Fr

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PAPATUI ANTIPERSPIRANT DEODORANT SANDALWOOD SUEDE 
aluminum zirconium trichlorohydrex gly stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83850-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (UNII: T27D6T99LH) (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY - UNII:T27D6T99LH)	ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY	16 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
COUMARIN (UNII: A4VZ22K1WT)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
LINALOOL, (+)- (UNII: F4VNO44C09)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
C15-19 ALKANE (UNII: CI87N1IM01)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
CETYL ALCOHOL (UNII: 936JST6JCN)
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
BALANITES AEGYPTIACA SEED OIL (UNII: 75T177G59E)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
DIMETHICONE (UNII: 92RU3N3Y1O)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83850-103-73	73 g in 1 CANISTER; Type 0: Not a Combination Product	01/15/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	01/15/2024

Labeler - Forward 7 (119133781)

Establishment
Name	Address	ID/FEI	Business Operations
KDC/One Development Corporation, Inc		204006464	manufacture(83850-103)