Lume Deodorant with Clinical Strength Sweat Control, Soft Powder 2.46 g/14g
Aluminum Sesquichlorohydrate · STICK · Lume Deodorant, LLC.
Lume Deodorant with Clinical Strength Sweat Control, Soft Powder is a stick containing aluminum sesquichlorohydrate at 2.46 g/14g, taken topical. Manufactured by Lume Deodorant, LLC..
Key Facts
- Brand Name
- Lume Deodorant with Clinical Strength Sweat Control, Soft Powder
- Generic Name
- Aluminum Sesquichlorohydrate
- NDC Code (Product)
84520-034- Manufacturer
- Lume Deodorant, LLC.
- Strength
- 2.46 g/14g
- Dosage Form
- STICK
- Route
- TOPICAL
- Marketing Status
- Application #
- M019
- Marketing Start
- 12/22/2025
Recall History
No Recall HistoryFrequently Asked Questions
What is Lume Deodorant with Clinical Strength Sweat Control, Soft Powder used for?
Lume Deodorant with Clinical Strength Sweat Control, Soft Powder contains Aluminum Sesquichlorohydrate. It is a stick taken topical. Consult your doctor for specific uses.
Is Lume Deodorant with Clinical Strength Sweat Control, Soft Powder a controlled substance?
Lume Deodorant with Clinical Strength Sweat Control, Soft Powder is not classified as a controlled substance by the DEA.
What is the generic name for Lume Deodorant with Clinical Strength Sweat Control, Soft Powder?
The generic name for Lume Deodorant with Clinical Strength Sweat Control, Soft Powder is Aluminum Sesquichlorohydrate. There are 12 other brand versions of Aluminum Sesquichlorohydrate.
What is the NDC code for Lume Deodorant with Clinical Strength Sweat Control, Soft Powder 2.46 g/14g?
The NDC (National Drug Code) for Lume Deodorant with Clinical Strength Sweat Control, Soft Powder 2.46 g/14g is 84520-034, listed by Lume Deodorant, LLC..
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)