DR SWEAT- aluminum chloride liquid 
Conopco Inc. d/b/a/ Unilever

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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Dr Sweat Clinical Strength Antiperspirant

DR SWEAT CLINICAL STRENGTH ANTIPERSPIRANT - aluminum chloride liquid

Dr Sweat Clinical Strength Antiperspirant

Drug Facts

Active ingredient

Aluminum Chloride (15.0%)

Purpose

Antiperspirant

Uses

• reduces underarm perspiration

Warnings

• For externaluse only.
• Do not use on broken skin .
• Ask a doctor before use if you have kidney disease.
• Stop use if rash or irritation occurs.

• Keep out of reach of children.

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

Directions

• Apply to underarms only
• Apply to clean dry underarms before going to bed.

Inactive ingredients

Water (Aqua), Tetrahydroxypropyl Ethylenediamine, VP/Polycarbamyl Polyglycol Ester, Phenoxyethanol, Polyacrylate Crosspolymer-6

Questions?

Call toll-free 866-269-6082

• Highest sweat profession available without a prescription
• Clinically tested and proven formula
• Simply and easy to apply
• No fragrance or alcohol
• Reduces sweat and odor

Packaging

DRSWEAT

DR SWEAT 
aluminum chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1633
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE15 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
EDETOL (UNII: Q4R969U9FR)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:64942-1633-10.0284 g in 1 PACKET; Type 0: Not a Combination Product03/29/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35003/29/2019
Labeler - Conopco Inc. d/b/a/ Unilever (001375088)

Revised: 12/2022
Document Id: ef3f84ad-9d66-b242-e053-2a95a90ac876
Set id: 822ef329-f042-54c4-e053-2991aa0ac753
Version: 2
Effective Time: 20221207
 
Conopco Inc. d/b/a/ Unilever