Advanced Herbal Care
NDC Package 23637-002-01

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Advanced Herbal Care is helps eliminate and reduces the recurrence of scalp itching, irritation, redness, flaking and scaling associated with dandruff. Marketed by B'iota Laboratories, this product is identified by NDC 23637-002 and is authorized under FDA application part358H.

Identification & Billing

NDC Package Code
23637-002-01
Package Description
1 BOTTLE in 1 CARTON / 300 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
23637000201

Clinical Specifications

Proprietary Name
Advanced Herbal Care For Thinning-damaged Hair
Dosage Form
-
Usage Information
Helps eliminate and reduces the recurrence of scalp itching, irritation, redness, flaking and scaling associated with dandruff.

Regulatory & Marketing

Labeler Name
B'iota Laboratories
FDA Application #
part358H
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
01-16-2018
Listing Expiration
12-31-2019
Exclude Flag
I
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 23637-002-01 identifies a specific commercial package of 1 bottle in 1 carton / 300 ml in 1 bottle of Advanced Herbal Care For Thinning-damaged Hair, labeled by B'iota Laboratories. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by B'iota Laboratories on January 16, 2018. The current certification is valid through December 31, 2019.

How is this B'iota Laboratories product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 23637000201. 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)
23637-002-01
11-Digit CMS (5-4-2)
23637-0002-01

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