Otc - Active Ingredient
Aluminum Zirconium Trichlorohydrex Gly 20%
Lume Deodorant With Clinical Strength Sweat Control Soft Powder Stick
FDA Label NDC 84520-036
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lume Deodorant, Llc for the product Lume Deodorant With Clinical Strength Sweat Control Soft Powder (NDC 84520-036). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - ask doctor, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiperspirant
Indications & Usage
Reduces underarm wetness
extra effective
Warnings
For external use only
Otc - Do Not Use
Do not use on broken skin
Otc - Ask Doctor
Ask a doctor before use if you have kidney disease
Otc - Stop Use
Stop use if rash or irritation occurs
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
Dosage & Administration
Apply to underamrs
Apply to dry skin
Apply at bedtime
Inactive Ingredient
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
* Please review the disclaimer below.
