FDA.reportPublic FDA data

Lume Deodorant with Clinical Strength Sweat Control Vanilla Bliss

Manufacturer
Lume Deodorant, LLC | Port Jervis Laboratories, Inc | KDC/One Development Corporation Inc.
Effective date
2026-08-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-08-08 02:01:51

Label at a glance#

ProductLume Deodorant with Clinical Strength Sweat Control Vanilla Bliss
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 or irritated 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 underarms only

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, Tetramethyl Acetyloctahydronaphthalenes, Vanallin, Trimethylcyclopentenyl Methylisopentenol, Benzyl Salicylate, Linalool, Coumarin, Anise Alcohol, Benzyl Benzoate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lume Deodorant with Clinical Strength Sweat Control Vanilla Bliss BackLume Deodorant with Clinical Strength Sweat Control Vanilla Bliss BackLume Deodorant with Clinical Strength Sweat Control Vanilla Bliss PDPLume Deodorant with Clinical Strength Sweat Control Vanilla Bliss PDP

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84520-03284520-032-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL724GKU717MIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
MANDELIC ACIDNH496X0UJXIACT
STEARYL ALCOHOL2KR89I4H1YIACT
WATER059QF0KO0RIACT
GINGERC5529G5JPQIACT
CITRONELLYL METHYLCROTONATEK61O222P3DIACT
DIMETHICONE92RU3N3Y1OIACT
DIHEPTYL SUCCINATE057N7SS26YIACT
MYRISTYL ALCOHOLV42034O9PUIACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
CETYL ALCOHOL936JST6JCNIACT
FRAGRANCE 135765EM498GW35IACT
ALLANTOIN344S277G0ZIACT
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)N7YC58165TIACT
TETRAMETHYL ACETYLOCTAHYDRONAPHTHALENES2JU6ZH6GREIACT
VANILLINCHI530446XIACT
EBANOL28N247O58BIACT
LINALOOLD81QY6I88EIACT
COUMARINA4VZ22K1WTIACT
ANISE ALCOHOL7N6XGV3U49IACT
BENZYL BENZOATEN863NB338GIACT
C15-19 ALKANECI87N1IM01IACT
BISABOLOL24WE03BX2TIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-07-27daily-update2026-08-04 03:33:25

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 Vanilla BlissALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYLume Deodorant, LLC561dd7a4-e30d-f369-e063-6294a90a61132026-08-03WarningsExact identifier
ndc (package): 84520-032-05
ndc (product): 84520-032
ndc11 (package): 84520003205
spl id: 5828b6d3-d4c5-9b81-e063-6394a90a5b87
spl set id: 561dd7a4-e30d-f369-e063-6294a90a6113

Reported adverse events (FAERS/openFDA)#

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