Babaria Oat Fresh Deodorant And Antiperspirant Liquid Roll-on Emulsion
NDC Package 78283-005-01

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

Package Information

Babaria Oat Fresh Deodorant And Antiperspirant Liquid Roll-on (aluminum chlorohydrate) emulsions is apply to underarms only. This formulation utilizes a emulsion delivery system. Marketed by Berioska Sl, this product is identified by NDC 78283-005 and is authorized under FDA application M019.

Identification & Billing

NDC Package Code
78283-005-01
Package Description
50 mL in 1 BOTTLE
Product Code
78283-005
11-Digit Billing Format
78283000501

Clinical Specifications

Proprietary Name
Babaria Oat Fresh Deodorant And Antiperspirant Liquid Roll-on
Non-Proprietary Name
Aluminum Chlorohydrate
Substance Name
Aluminum Chlorohydrate
Dosage Form
Emulsion - A dosage form consisting of a two-phase system comprised of at least two immiscible liquids1, one of which is dispersed as droplets (internal or dispersed phase) within the other liquid (external or continuous phase), generally stabilized with one or more emulsifying agents. (Note: Emulsion is used as a dosage form term unless a more specific term is applicable, e.g. cream, lotion, ointment.)
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 200 mg/mL
Usage Information
Apply to underarms only

Regulatory & Marketing

Labeler Name
Berioska Sl
Product Type
Human Otc Drug
FDA Application #
M019
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-18-2024
End Marketing Date
01-01-2030
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 78283-005-01 identifies a specific commercial package of 50 ml in 1 bottle of Babaria Oat Fresh Deodorant And Antiperspirant Liquid Roll-on, a human over the counter drug labeled by Berioska Sl. This emulsion 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 Berioska Sl on March 18, 2024.

How is this Berioska Sl product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 78283000501. 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)
78283-005-01
11-Digit CMS (5-4-2)
78283-0005-01

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