ANTIPERSPIRANT FOR HANDS FEET BODY  ZERO SWEAT- aluminum sesquichlorohydrate lotion 
Zero Sweat 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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Antiperspirant Lotion for Hands Feet Body
Zero Sweat®

Drug Facts

Active Ingredient

Aluminum Sesquichlorohydrate

Purpose

Antiperspirant

Uses

Warnings

For external use only

Do Not Use

on irritated skin

  • On irritated skin

Stop use and ask a doctor if rash or irritation develops

Ask a doctor before use if you have kidney disease

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

Water,Steareth-2, Aluminum Starch Octenyl Succinate, Steareth-20, PPG-15 Stearyl Ether, Isopropyl Myristate, Dimethicone

Questions?

Email dry@zerosweat.com

Distributed by ZeroSweat Inc.

www.ZeroSweat.com

PRINCIPAL DISPLAY PANEL - 40 ml Tube Box

ZERO Z SWEAT®

Keeps You Dry.

Antiperspirant
Lotion

For Hands, Feet, Body

1.35 FL. OZ. (40 ml.)

Principal Display Panel - 40 ml Tube Box
ANTIPERSPIRANT FOR HANDS FEET BODY   ZERO SWEAT
aluminum sesquichlorohydrate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55726-293
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Aluminum Sesquichlorohydrate (UNII: UCN889409V) (Aluminum Sesquichlorohydrate - UNII:UCN889409V) Aluminum Sesquichlorohydrate150 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Steareth-2 (UNII: V56DFE46J5)  
Aluminum starch Octenylsuccinate (UNII: I9PJ0O6294)  
Steareth-20 (UNII: L0Q8IK9E08)  
PPG-15 Stearyl Ether (UNII: 1II18XLS1L)  
Isopropyl Myristate (UNII: 0RE8K4LNJS)  
Dimethicone (UNII: 92RU3N3Y1O)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55726-293-401 in 1 BOX, UNIT-DOSE09/15/2017
140 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35009/15/2017
Labeler - Zero Sweat Inc. (078507610)
Registrant - BMC 1092, Inc. dba Solo Laboratories, Inc (078831987)
Establishment
NameAddressID/FEIBusiness Operations
BMC 1092, Inc. dba Solo Laboratories, Inc078831987MANUFACTURE(55726-293) , PACK(55726-293)

Revised: 1/2020
Document Id: 889f39b3-63d9-4ac0-8629-556b7ba63e73
Set id: 9c3f9b2e-590a-4a73-a037-c5ba871d5b88
Version: 2
Effective Time: 20200110
 
Zero Sweat Inc.