UNDERARM ANTIPERSPIRANT DAILY USE FRESH LINEN SCENT- aluminum zirconium tetrachlorohydrex gly stick

Underarm Antiperspirant Daily Use Fresh Linen Scent by

Drug Labeling and Warnings

Underarm Antiperspirant Daily Use Fresh Linen Scent by is a Otc medication manufactured, distributed, or labeled by Clutch Inc, Wasatch Product Development, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient Purpose

Aluminum Zirconium Tetrachlorohydrex Gly (20%) Antiperspirant

PURPOSE

Use

reduces underarm perspiration

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Stop use if rash or irritation occurs

WARNINGS

Warnings

For external use only. Do not use on broken skin

DOSAGE & ADMINISTRATION

DIrections

apply before bed and again in morning

apply to underarm only

INACTIVE INGREDIENT

Inactive ingredients

Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, Dicaprylyl Carbonate, Fragrance, Hydrogenated Castor Oil, Isopropyl Myristate, Lauryl Methacrylate/Glycol Dimethacrylate Crosspolymer, PEG-8 Distearate, Silica, Propylene Glycol, Ethylhexylglycerin, Maranta Arundinacea Root Extract, Coconut Alkanes, Charcoal Powder, Octenidine Hydrochloride, Coco-Caprylate/Caprate.

PRINCIPAL DISPLAY PANEL

Carpe

Clinical Grade

Underarm

Antiperspirant

Daily Use Fresh Linen Scent

Net Wt 2 OZ (58 G)

INGREDIENTS AND APPEARANCE

UNDERARM ANTIPERSPIRANT DAILY USE FRESH LINEN SCENT 
aluminum zirconium tetrachlorohydrex gly stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74307-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE)	ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY	20 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
LAURYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EX0F4CZ66H)
MARANTA ARUNDINACEA ROOT (UNII: FVN346W31A)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
PEG-8 DISTEARATE (UNII: 7JNC8VN07M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
COCONUT ALKANES (UNII: 1E5KJY107T)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
OCTENIDINE HYDROCHLORIDE (UNII: U84956NU4B)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74307-009-01	58 g in 1 CONTAINER; Type 0: Not a Combination Product	10/19/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	10/19/2021

Labeler - Clutch Inc (080214892)

Establishment
Name	Address	ID/FEI	Business Operations
Wasatch Product Development, LLC.		962452533	manufacture(74307-009)