Noavia Pore Firming Serum Liquid
NDC Package 85212-0013-1

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

Package Information

Noavia Pore Firming Serum (field mushroom, hamamelis virginiana (witch hazel) leaf water) liquids is bOTANICAL PURITY FOR A YOUTHFUL COMPLEXIONSOOTHES, PROTECTS, AND BALANCES SENSITIVE SKINIt relieves dry, flaky skin and protects against irritation and harmful microbes, restoring balance to your skin. This formulation utilizes a liquid delivery system. Marketed by Beijing Junge Technology Co., Ltd., this product is identified by NDC 85212-0013 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
85212-0013-1
Package Description
30 mL in 1 BOTTLE
Product Code
85212-0013
11-Digit Billing Format
85212001301

Clinical Specifications

Proprietary Name
Noavia Pore Firming Serum
Non-Proprietary Name
Field Mushroom, Hamamelis Virginiana (witch Hazel) Leaf Water
Substance Name
Field Mushroom; Hamamelis Virginiana (witch Hazel) Leaf Water
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
Extracorporeal - Administration outside of the body.
Active Ingredient(s)
Usage Information
BOTANICAL PURITY FOR A YOUTHFUL COMPLEXIONSOOTHES, PROTECTS, AND BALANCES SENSITIVE SKINIt relieves dry, flaky skin and protects against irritation and harmful microbes, restoring balance to your skin.

Regulatory & Marketing

Labeler Name
Beijing Junge Technology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-01-2024
Listing Expiration
12-31-2026
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 85212-0013-1 identifies a specific commercial package of 30 ml in 1 bottle of Noavia Pore Firming Serum, a human over the counter drug labeled by Beijing Junge Technology Co., Ltd.. This liquid is formulated for extracorporeal use and contains field mushroom; hamamelis virginiana (witch hazel) leaf water 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 Beijing Junge Technology Co., Ltd. on September 01, 2024. The current certification is valid through December 31, 2026.

How is this Beijing Junge Technology Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85212001301. 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)
85212-0013-1
11-Digit CMS (5-4-2)
85212-0013-01

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