Lume Deodorant With Clinical Strength Sweat Control, Soft Powder Stick
NDC Package 84520-034-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Lume Deodorant With Clinical Strength Sweat Control, Soft Powder (aluminum sesquichlorohydrate) sticks is apply to underarms onlyapply to dry skinapply at bedtime. This formulation utilizes a stick delivery system. Marketed by Lume Deodorant, Llc., this product is identified by NDC 84520-034 and is authorized under FDA application M019.

Identification & Billing

NDC Package Code
84520-034-01
Package Description
14 g in 1 CONTAINER
Product Code
84520-034
11-Digit Billing Format
84520003401

Clinical Specifications

Proprietary Name
Lume Deodorant With Clinical Strength Sweat Control, Soft Powder
Non-Proprietary Name
Aluminum Sesquichlorohydrate
Substance Name
Aluminum Sesquichlorohydrate
Dosage Form
Stick - A dosage form prepared in a relatively long and slender often cylindrical form.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
ALUMINUM SESQUICHLOROHYDRATE 2.46 g/14g
Usage Information
Apply to underarms onlyapply to dry skinapply at bedtime

Regulatory & Marketing

Labeler Name
Lume Deodorant, Llc.
Product Type
Human Otc Drug
FDA Application #
M019
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-22-2025
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 84520-034-01 identifies a specific commercial package of 14 g in 1 container of Lume Deodorant With Clinical Strength Sweat Control, Soft Powder, a human over the counter drug labeled by Lume Deodorant, Llc.. This stick is formulated for topical use and contains aluminum sesquichlorohydrate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Lume Deodorant, Llc. on December 22, 2025. The current certification is valid through December 31, 2027.

How is this Lume Deodorant, Llc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84520003401. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
84520-034-01
11-Digit CMS (5-4-2)
84520-0034-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.