Dr Sweat

Manufacturer: Conopco Inc. d/b/a/ Unilever
Effective date: 2022-12-07
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:52:09

Label at a glance#

ProductDr Sweat

Active ingredientALUMINUM CHLORIDE

Label structure11 sections

Indications and uses

• reduces underarm perspiration

Dosage and administration

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

Contacts and useful links#

PhoneLabel contact866-269-6082

Label contents#

Full prescribing information#

DR SWEAT CLINICAL STRENGTH ANTIPERSPIRANT - aluminum chloride liquid

DESCRIPTION SECTION

Dr Sweat Clinical Strength Antiperspirant

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Chloride (15.0%)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

• reduces underarm perspiration

Warnings

WARNINGS SECTION

• 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children.

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DRSWEAT

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64942-1633-1	2025-01-30	C162847	48780-1	2cef2736-8b9b-d83d-e063-dadaa90ab31f	Dr Sweat Clinical Strength Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64942-1633-1	Dr Sweat	0.0284 g in 1 PACKET	LIQUID	0.0284		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64942-1633	DR SWEAT (ALUMINUM CHLORIDE) LIQUID [CONOPCO INC. D/B/A/ UNILEVER]	2	Legacy NDC, 1 package rows	20221208_822ef329-f042-54c4-e053-2991aa0ac753.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

Dr Sweat
Aluminum Chloride
WATER
EDETOL
PHENOXYETHANOL
ALUMINUM CATION
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64942-1633	64942-1633-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
EDETOL	Q4R969U9FR	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
ALUMINUM CHLORIDE	3CYT62D3GA	ACTIB
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S)	Q7UI015FF9	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ef3f84ad-9d66-b242-e053-2a95a90ac876			822ef329-f042-54c4-e053-2991aa0ac753	2022-12-07	Warnings	Exact identifier spl id: ef3f84ad-9d66-b242-e053-2a95a90ac876 spl set id: 822ef329-f042-54c4-e053-2991aa0ac753

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.