FDA.reportPublic FDA data

Shaklee Essentials Desert Wind Roll-On Antiperspirant

Manufacturer
Shaklee Corporation
Effective date
2022-10-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:50:52

Label at a glance#

ProductShaklee Essentials Desert Wind Roll-On Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure6 sections

Dosage and administration

Tip bottle and roll on. Apply to underarms only.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate (Anhydrous) 16%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

This product is used to decrease underarm wetness.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on broken skin. 

Stop use if

OTC - STOP USE SECTION

rash or irritation occurs.

Ask your doctor before use if you have

OTC - ASK DOCTOR SECTION

kidney disease.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

  • Tip bottle and roll on.
  • Apply to underarms only.

Cosmetic Ingredients:

INACTIVE INGREDIENT SECTION

Water, Glyceryl Stearate, PEG-100 Stearate, Ethylhexyl Palmitate, Isopropyl Myristate, Glycerin, Petrolatum, Cyclotetrasiloxane, PEG-5 Soy Sterol, Dimethyl Sebacate, Isopropyl Lanolate, Allantoin, Cetyl Alcohol, Magnesium Aluminum Silicate, Lanolin Alcohol, Cyclopentasiloxane, Frageance.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59899-014-0059899-014-00

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59899-02059899-020-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
ETHYLHEXYL PALMITATE2865993309IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
GLYCERINPDC6A3C0OXIACT
PETROLATUM4T6H12BN9UIACT
CYCLOMETHICONE 4CZ227117JEIACT
PEG-5 SOY STEROLJE4505562OIACT
DIMETHYL SEBACATEG87745M355IACT
ALLANTOIN344S277G0ZIACT
CETYL ALCOHOL936JST6JCNIACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
LANOLIN ALCOHOLS884C3FA9HEIACT
CYCLOMETHICONE 50THT5PCI0RIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ebe12e78-b8c1-0f12-e053-2a95a90aa73c63f0ba74-c7f4-428f-e053-2991aa0a740e2022-10-25WarningsExact identifier
spl id: ebe12e78-b8c1-0f12-e053-2a95a90aa73c
spl set id: 63f0ba74-c7f4-428f-e053-2991aa0a740e

Reported adverse events (FAERS/openFDA)#

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