STEARYL ALCOHOL - Lume Deodorant, LLC | KDC/One Development Corporation Inc.

Manufacturer
Lume Deodorant, LLC | KDC/One Development Corporation Inc.
Effective date
2026-07-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-04 03:33:36

Label at a glance#

ProductLume Deodorant with Clinical Strength Sweat Control Soft Powder
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Trichlorohydrex Gly 20%

OTC - PURPOSE SECTION

Antiperspirant

INDICATIONS & USAGE SECTION

Reduces underarm wetness

extra effective

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

OTC - STOP USE SECTION

Stop use if rash or irritation occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

Apply to underamrs

Apply to dry skin

Apply at bedtime

INACTIVE INGREDIENT SECTION

Stearyl Alcohol, Dimethicone, C15-19 Alkane, Diheptyl Succinate, Water/Aqua/Eau, C12-15 Alkyl Benzoate, Hydrogenated Castor Oil, Cetyl Alcohol, Silica, Fragrance/Parfum, Aluminum Starch Octenylsuccinate, Mandelic Acid, Bisabolol, Allantoin, Tocopheryl Acetate, Simmondsia Chinensis (Jojoba) Seed Oil, Zingiber Officinale (Ginger) Root Extract, Capryloyl Glycerin/Sebacic Acid Copolymer, Myristyl Alcohol, Citronellyl Methylcrotonate, Geraniol, Tetramethyl Acetyloctahydronaphthalenes, Alpha-Isomethyl Ionone, Citronellol, Geranyl Acetate, Citral

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lume Deodorant with Clinical Strength Sweat Control Soft Powder LabelLume Deodorant with Clinical Strength Sweat Control Soft Powder LabelLume Deodorant with Clinical Strength Sweat Control Soft Powder LabelLume Deodorant with Clinical Strength Sweat Control Soft Powder Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850042058725GTIN-13: 0850042058725
EAN-13: 0850042058725
GTIN-12: 850042058725
UPC-A: 850042058725
GTIN storage (14 digits): 00850042058725
US_AP Deo Sweat Control Solid Stick 2.6oz Soft Powder BOP_OL.jpg

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84520-03684520-036-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

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
Lume Deodorant with Clinical Strength Sweat Control Soft PowderALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYLume Deodorant, LLC561d4592-79e6-105b-e063-6394a90a52f02026-07-08WarningsExact identifier
ndc (package): 84520-036-05
ndc (product): 84520-036
ndc11 (package): 84520003605
spl id: 561d4592-79e7-105b-e063-6394a90a52f0
spl set id: 561d4592-79e6-105b-e063-6394a90a52f0

Reported adverse events (FAERS/openFDA)#

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