Lyophilized Amnion With Albumin Powder, For Solution
NDC Package 74458-238-01

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

Package Information

Lyophilized Amnion With Albumin (human amniotic membrane) powders is uses: temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: sneezing runny nose itchy, watery eyes itchy throat. This formulation utilizes a powder, for solution delivery system. Marketed by Guangzhou Yilong Cosmetics.,ltd, this product is identified by NDC 74458-238 and is authorized under FDA application M001.

Identification & Billing

NDC Package Code
74458-238-01
Package Description
10 mg in 1 BOTTLE
Product Code
74458-238
11-Digit Billing Format
74458023801

Clinical Specifications

Proprietary Name
Lyophilized Amnion With Albumin
Non-Proprietary Name
Human Amniotic Membrane
Substance Name
Human Amniotic Membrane
Dosage Form
Powder, For Solution - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a solution.
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)
HUMAN AMNIOTIC MEMBRANE 2 mg/100mg
Usage Information
Uses: temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: sneezing runny nose itchy, watery eyes itchy throat

Regulatory & Marketing

Labeler Name
Guangzhou Yilong Cosmetics.,ltd
Product Type
Human Otc Drug
FDA Application #
M001
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-11-2026
Listing Expiration
12-31-2027
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 74458-238-01 identifies a specific commercial package of 10 mg in 1 bottle of Lyophilized Amnion With Albumin, a human over the counter drug labeled by Guangzhou Yilong Cosmetics.,ltd. This powder, for solution is formulated for topical use and contains human amniotic membrane 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 Guangzhou Yilong Cosmetics.,ltd on July 11, 2026. The current certification is valid through December 31, 2027.

How is this Guangzhou Yilong Cosmetics.,ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 74458023801. 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)
74458-238-01
11-Digit CMS (5-4-2)
74458-0238-01

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