Dove Aerosol, Spray
NDC Package 64942-2139-2

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

Package Information

Dove (even tone plus niacinamide peach blossom and rice milk dry spray 72h antiperspirant deodorant) aerosols is apply to underarms only. This formulation utilizes a aerosol, spray delivery system. Marketed by Conopco, Inc. D/b/a Unilever, this product is identified by NDC 64942-2139 and is authorized under FDA application M019.

Identification & Billing

NDC Package Code
64942-2139-2
Package Description
28 g in 1 CAN
Product Code
64942-2139
11-Digit Billing Format
64942213902

Clinical Specifications

Proprietary Name
Dove
Non-Proprietary Name
Even Tone Plus Niacinamide Peach Blossom And Rice Milk Dry Spray 72h Antiperspirant Deodorant
Substance Name
Aluminum Sesquichlorohydrate
Dosage Form
Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous 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)
ALUMINUM SESQUICHLOROHYDRATE 12.2 g/100g
Usage Information
Apply to underarms only

Regulatory & Marketing

Labeler Name
Conopco, Inc. D/b/a Unilever
Product Type
Human Otc Drug
FDA Application #
M019
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-10-2023
Listing Expiration
12-31-2026
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (64942-2139). Click a package code to view its specific billing and regulatory data.

64942-2139-1
107 g in 1 CAN

* 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 64942-2139-2 identifies a specific commercial package of 28 g in 1 can of Dove, a human over the counter drug labeled by Conopco, Inc. D/b/a Unilever. This aerosol, spray 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 Conopco, Inc. D/b/a Unilever on July 10, 2023. The current certification is valid through December 31, 2026.

How is this Conopco, Inc. D/b/a Unilever product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 64942213902. 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)
64942-2139-2
11-Digit CMS (5-4-2)
64942-2139-02

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