Mdp Peptide 9 Bio Sun Pro Stick
NDC Package 72220-002-04

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

Package Information

Mdp Peptide 9 Bio Sun Pro (homosalate, octocrylene, ethylhexyl salicylate, butyl methoxydibenzoylmethane) sticks is use(s)■ Helps prevent sunburn■ If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun. This formulation utilizes a stick delivery system. Marketed by Skinidea Co., Ltd, this product is identified by NDC 72220-002 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
72220-002-04
Package Description
1 CONTAINER in 1 CARTON / 20 g in 1 CONTAINER (72220-002-03)
Product Code
72220-002
11-Digit Billing Format
72220000204

Clinical Specifications

Proprietary Name
Mdp Peptide 9 Bio Sun Pro
Non-Proprietary Name
Homosalate, Octocrylene, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane
Substance Name
Avobenzone; Homosalate; Octisalate; Octocrylene
Dosage Form
Stick - A dosage form prepared in a relatively long and slender often cylindrical form.
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)
Usage Information
Use(s)■ Helps prevent sunburn■ If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Regulatory & Marketing

Labeler Name
Skinidea Co., Ltd
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-01-2024
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (72220-002). Click a package code to view its specific billing and regulatory data.

72220-002-02
1 CONTAINER in 1 CARTON / 20 g in 1 CONTAINER (72220-002-01)

* 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 72220-002-04 identifies a specific commercial package of 1 container in 1 carton / 20 g in 1 container (72220-002-03) of Mdp Peptide 9 Bio Sun Pro, a human over the counter drug labeled by Skinidea Co., Ltd. This stick is formulated for topical use and contains avobenzone; homosalate; octisalate; octocrylene 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 Skinidea Co., Ltd on November 01, 2024. The current certification is valid through December 31, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72220000204. 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)
72220-002-04
11-Digit CMS (5-4-2)
72220-0002-04

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