Antiperspirant Deodorant Extra Dry Men Lotion
NDC Package 53675-200-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Antiperspirant Deodorant Extra Dry Men (aluminum chlorohydrate) lotions is apply to underarms only. This formulation utilizes a lotion delivery system. Marketed by Aruba Aloe Balm Nv, this product is identified by NDC 53675-200 and is authorized under FDA application M019.

Identification & Billing

NDC Package Code
53675-200-01
Package Description
89 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
53675020001

Clinical Specifications

Proprietary Name
Antiperspirant Deodorant Extra Dry Men
Non-Proprietary Name
Aluminum Chlorohydrate
Substance Name
Aluminum Chlorohydrate
Dosage Form
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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)
Usage Information
Apply to underarms only.

Regulatory & Marketing

Labeler Name
Aruba Aloe Balm Nv
Product Type
Human Otc Drug
FDA Application #
M019
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-24-2022
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

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 53675-200-01 identifies a specific commercial package of 89 ml in 1 bottle of Antiperspirant Deodorant Extra Dry Men, a human over the counter drug labeled by Aruba Aloe Balm Nv. This lotion is formulated for topical use and contains aluminum chlorohydrate 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 Aruba Aloe Balm Nv on February 24, 2022. The current certification is valid through December 31, 2026.

How is this Aruba Aloe Balm Nv product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 53675020001. 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)
53675-200-01
11-Digit CMS (5-4-2)
53675-0200-01

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