Huitomi Pack
NDC Package 69388-6001-1

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.

Huitomi Pack is use morning and evening after washing two times mostly Because makeup base is possible with these serum and cream, makeup for other moisturizing products does not need.The serum used first and then using the cream. Marketed by Lancell Bio Co., Ltd., this product is identified by NDC 69388-6001 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
69388-6001-1
Package Description
50 mL in 1 BOTTLE
Product Code
69388-6001
11-Digit Billing Format
69388600101

Clinical Specifications

Proprietary Name
Huitomi Pack
Dosage Form
-
Usage Information
Use morning and evening after washing two times mostly Because makeup base is possible with these serum and cream, makeup for other moisturizing products does not need.The serum used first and then using the cream. Apply serum in face and serum tap lightly with palm until is absorbed in skin.Apply cream in face and massage lightly with palm until cream is assimilated in skin.Use is possible to atopic sensitive skin or young infant because composition antiseptic of minimum quantity was contained to serum and there is no composition antiseptic to cream

Regulatory & Marketing

Labeler Name
Lancell Bio Co., Ltd.
FDA Application #
part347
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
04-20-2015
Listing Expiration
12-31-2017
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 69388-6001-1 identifies a specific commercial package of 50 ml in 1 bottle of Huitomi Pack, labeled by Lancell Bio Co., Ltd.. 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 Lancell Bio Co., Ltd. on April 20, 2015. The current certification is valid through December 31, 2017.

How is this Lancell Bio Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69388600101. 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)
69388-6001-1
11-Digit CMS (5-4-2)
69388-6001-01

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