Sweatblock Solution
NDC Package 54913-011-10

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

Package Information

Sweatblock (aluminum chloride) solution is a medication used to help control excessive sweating. This formulation utilizes a solution delivery system. Marketed by Dc Alpine Partners, Llc, this product is identified by NDC 54913-011 and is authorized under FDA application M019.

Identification & Billing

NDC Package Code
54913-011-10
Package Description
10 PACKET in 1 BOX / 3 mL in 1 PACKET
Product Code
11-Digit Billing Format
54913001110

Clinical Specifications

Proprietary Name
Sweatblock Original Maximum Clinical Protection
Non-Proprietary Name
Aluminum Chloride
Substance Name
Aluminum Chloride
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
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
This medication is used to help control excessive sweating.

Regulatory & Marketing

Labeler Name
Dc Alpine Partners, Llc
Product Type
Human Otc Drug
FDA Application #
M019
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-01-2026
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 54913-011-10 identifies a specific commercial package of 10 packet in 1 box / 3 ml in 1 packet of Sweatblock Original Maximum Clinical Protection, a human over the counter drug labeled by Dc Alpine Partners, Llc. This solution is formulated for topical use and contains aluminum chloride 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 Dc Alpine Partners, Llc on January 01, 2026. The current certification is valid through December 31, 2027.

What are the primary indications for this medication?

This medication is used to help control excessive sweating.

How is this Dc Alpine Partners, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54913001110. 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)
54913-011-10
11-Digit CMS (5-4-2)
54913-0011-10

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