HAND ANTIPERSPIRANT NIGHTLY USE- aluminum chloride hexahydrate cream

Hand Antiperspirant Nightly Use by

Drug Labeling and Warnings

Hand Antiperspirant Nightly Use 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 Chloride Hexahydrate (15%) Anti-perspirant

PURPOSE

Use

• reduces 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 and ask a doctor if rash or irritation occurs

WARNINGS

Warnings

For external use only.

Do not use on broken or irritated skin

Ask a doctor before use if you have kidney disease.

DOSAGE & ADMINISTRATION

Directions

Wash and dry hands thoroughly before application
Apply a single pump of product to palms each morning
Rub palms together vigorously for 30 seconds

INACTIVE INGREDIENT

Inactive Ingredients Aluminum Starch Octenylsuccinate, Aqua (water), Cetyl Hydroxyethylcellulose, Coco-Caprylate/Caprate,Coconut Alkanes, Disodium EDTA, Ethylhexylglycerin, Glycerin, Helianthus Annuus (Suflower) Extract, Hydroxypropyl Starch Phosphate, Octenidine HCL, Oryza Sativa (Rice) Bran Extract, Phenoxyethanol, Polymethylsilsesquioxane, Propanediol, Propylene Glycol, Rosmarinus Officinalis (Rosemary) Leaf Extract, SD Alcohol 40-B, SIlica, Sodium Hydroxide, Tocopherol, Xanthan Gum

PRINCIPAL DISPLAY PANEL

Carpe

Clinical Grade HAND

Antiperspirant

Nightly Use

15% Aluminum Chloride

INGREDIENTS AND APPEARANCE

HAND ANTIPERSPIRANT NIGHTLY USE 
aluminum chloride hexahydrate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74307-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B)	ALUMINUM CHLORIDE	15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
OCTENIDINE HYDROCHLORIDE (UNII: U84956NU4B)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
COCONUT ALKANES (UNII: 1E5KJY107T)
COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
WATER (UNII: 059QF0KO0R)
CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)
TOCOPHEROL (UNII: R0ZB2556P8)
XANTHAN GUM (UNII: TTV12P4NEE)
ROSEMARY (UNII: IJ67X351P9)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
RICE BRAN (UNII: R60QEP13IC)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPANEDIOL (UNII: 5965N8W85T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74307-008-01	30 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	06/01/2020

Labeler - Clutch Inc (080214892)

Establishment
Name	Address	ID/FEI	Business Operations
Wasatch Product Development, LLC.		962452533	manufacture(74307-008)