FDA.reportPublic FDA data

Shaklee Essentials Antiperspirant Cream

Manufacturer
Shaklee Corporation
Effective date
2022-10-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:50:53

Label at a glance#

ProductAntiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure6 sections

Dosage and administration

Smooth on small amount with fingertips. 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

If swallowed, get medical help or contact a poison control center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Smooth on small amount with fingertips.
  • Apply to underarms only.

Cosmetic Ingredients:

INACTIVE INGREDIENT SECTION

Water, Cetyl Alcohol, Propylene Glycol, Glyceryl Stearate, PEG-100 Stearate, Squalane, Fragrance.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59899-015-00 259899-015-00 2

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59899-02159899-021-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CETYL ALCOHOL936JST6JCNIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
SQUALANEGW89575KF9IACT
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
ebe0e6f8-453a-6be1-e053-2995a90ad33063f11407-46d5-3314-e053-2991aa0a37342022-10-25WarningsExact identifier
spl id: ebe0e6f8-453a-6be1-e053-2995a90ad330
spl set id: 63f11407-46d5-3314-e053-2991aa0a3734

Reported adverse events (FAERS/openFDA)#

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