Celistar Microneedling Infusion Liquid
NDC Package 87765-001-01

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

Package Information

Celistar Microneedling Infusion (hyaluronate sodium) liquids is a medication used to protect skin ulcers, burns, or wounds from irritation so that the skin can heal properly. This formulation utilizes a liquid delivery system. Marketed by Guangdong Outeli Biotechnology Co., Ltd., this product is identified by NDC 87765-001 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
87765-001-01
Package Description
20 mL in 1 BOX
Product Code
11-Digit Billing Format
87765000101

Clinical Specifications

Proprietary Name
Celistar Microneedling Infusion
Non-Proprietary Name
Hyaluronate Sodium
Substance Name
Hyaluronate Sodium; Hydrolysed Marine Collagen (enzymatic; 2000 Mw)
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.
Usage Information
This medication is used to protect skin ulcers, burns, or wounds from irritation so that the skin can heal properly. Some products are also used to help relieve itching and pain from various skin conditions. Hyaluronate is the same as a natural substance that is found in your body. It works by forming a protective layer over the affected area.

Regulatory & Marketing

Labeler Name
Guangdong Outeli Biotechnology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-10-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (87765-001). Click a package code to view its specific billing and regulatory data.

10 mL in 1 BOX

* 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 87765-001-01 identifies a specific commercial package of 20 ml in 1 box of Celistar Microneedling Infusion, a human over the counter drug labeled by Guangdong Outeli Biotechnology Co., Ltd.. This liquid is formulated for topical use and contains hyaluronate sodium; hydrolysed marine collagen (enzymatic; 2000 mw) 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 Guangdong Outeli Biotechnology Co., Ltd. on June 10, 2026. The current certification is valid through December 31, 2027.

What are the primary indications for this medication?

This medication is used to protect skin ulcers, burns, or wounds from irritation so that the skin can heal properly. Some products are also used to help relieve itching and pain from various skin conditions. Hyaluronate is the same as a natural substance that is found in your body. It works by forming a protective layer over the affected area.

How is this Guangdong Outeli Biotechnology Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87765000101. 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)
87765-001-01
11-Digit CMS (5-4-2)
87765-0001-01

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