African Sea-coconut
NDC Package 64272-736-01

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

Package Information

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

African Sea-coconut is use only as directedadults and children 12 years and oldertake orally 2 to 4 teaspoons (10-20mL) every 4 hours, not to exceed 24 teaspoons in 24 hours.children 6 to under 12 yearstake 1 to 2 teaspoons (5-10mL) every 4 hours, not to exceed 12 teaspoons in 24 hours.children under 6 yearsconsult a doctor before use. Marketed by Luen Fook Medicine Sdn. Bhd., this product is identified by NDC 64272-736 and is authorized under FDA application part356.

Identification & Billing

NDC Package Code
64272-736-01
Package Description
1 BOTTLE, GLASS in 1 BOX / 177 mL in 1 BOTTLE, GLASS
Product Code
64272-736
11-Digit Billing Format
64272073601

Clinical Specifications

Proprietary Name
African Sea-coconut Herbal Mixture
Dosage Form
-
Usage Information
Use only as directedadults and children 12 years and oldertake orally 2 to 4 teaspoons (10-20mL) every 4 hours, not to exceed 24 teaspoons in 24 hours.children 6 to under 12 yearstake 1 to 2 teaspoons (5-10mL) every 4 hours, not to exceed 12 teaspoons in 24 hours.children under 6 yearsconsult a doctor before use.

Regulatory & Marketing

Labeler Name
Luen Fook Medicine Sdn. Bhd.
FDA Application #
part356
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
12-20-2011
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 64272-736-01 identifies a specific commercial package of 1 bottle, glass in 1 box / 177 ml in 1 bottle, glass of African Sea-coconut Herbal Mixture, labeled by Luen Fook Medicine Sdn. Bhd.. 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 Luen Fook Medicine Sdn. Bhd. on December 20, 2011. The current certification is valid through December 31, 2019.

How is this Luen Fook Medicine Sdn. Bhd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 64272073601. 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)
64272-736-01
11-Digit CMS (5-4-2)
64272-0736-01

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