DR SWEAT- aluminum chloride liquid

Dr Sweat by

Drug Labeling and Warnings

Dr Sweat by is a Otc medication manufactured, distributed, or labeled by Conopco Inc. d/b/a/ Unilever. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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

OTHER SAFETY INFORMATION

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

INGREDIENTS AND APPEARANCE

DR SWEAT 
aluminum chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1633
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 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-1633-1	0.0284 g in 1 PACKET; Type 0: Not a Combination Product	03/29/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	03/29/2019

Labeler - Conopco Inc. d/b/a/ Unilever (001375088)