Dawnmist Antiperspirant Deodorant Lotion
NDC Package 65517-1021-1

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

Package Information

Dawnmist Antiperspirant Deodorant (aluminum chlorohydrate) lotions is apply to underarms only. This formulation utilizes a lotion delivery system. Marketed by Dukal Llc, this product is identified by NDC 65517-1021 and is authorized under FDA application M019.

Identification & Billing

NDC Package Code
65517-1021-1
Package Description
44 mL in 1 BOTTLE, WITH APPLICATOR
Product Code
65517-1021
11-Digit Billing Format
65517102101

Clinical Specifications

Proprietary Name
Dawnmist Antiperspirant Deodorant
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)
ALUMINUM CHLOROHYDRATE 78 mg/mL
Usage Information
Apply to underarms only.

Regulatory & Marketing

Labeler Name
Dukal Llc
Product Type
Human Otc Drug
FDA Application #
M019
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-12-2018
End Marketing Date
03-25-2027
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 65517-1021-1 identifies a specific commercial package of 44 ml in 1 bottle, with applicator of Dawnmist Antiperspirant Deodorant, a human over the counter drug labeled by Dukal Llc. 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 Dukal Llc on October 12, 2018.

How is this Dukal Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 65517102101. 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 (5-4-1)
65517-1021-1
11-Digit CMS (5-4-2)
65517-1021-01

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