HAND ANTIPERSPIRANT NIGHTLY USE- aluminum chloride hexahydrate cream 
Clutch Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Hand Antiperspirant Nightly Use

Active Ingredient Purpose

Aluminum Chloride Hexahydrate (15%) Anti-perspirant

Use

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

Stop use and ask a doctor if rash or irritation occurs

Warnings

For external use only.

Do not use on broken or irritated skin

Ask a doctor before use if you have kidney disease.

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 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

Carpe

Clinical Grade HAND

Antiperspirant

Nightly Use

15% Aluminum Chloride

Nightly Use Carpe

HAND ANTIPERSPIRANT NIGHTLY USE 
aluminum chloride hexahydrate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74307-008
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE15 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74307-008-0130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35006/01/2020
Labeler - Clutch Inc (080214892)
Establishment
NameAddressID/FEIBusiness Operations
Wasatch Product Development, LLC.962452533manufacture(74307-008)

Revised: 6/2020
Document Id: a70d9eff-b5a4-5c52-e053-2a95a90a704c
Set id: a70d9eff-b5a3-5c52-e053-2a95a90a704c
Version: 1
Effective Time: 20200601
 
Clutch Inc