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  5. NDC Package Code: 72220-002-04 Mdp Peptide 9 Bio Sun Pro

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

Homosalate,Octocrylene,Ethylhexyl Salicylate,Butyl Methoxydibenzoylmethane Stick Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

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
Proprietary Name:
Mdp Peptide 9 Bio Sun Pro
Non-Proprietary Name:
Homosalate, Octocrylene, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane
Substance Name:
Avobenzone; Homosalate; Octisalate; Octocrylene
Usage Information:
Use(s)â–  Helps prevent sunburnâ–  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
11-Digit NDC Billing Format:
72220000204
Product Type:
Human Otc Drug
Labeler Name:
Skinidea Co., Ltd
Dosage Form:
Stick - A dosage form prepared in a relatively long and slender often cylindrical form.
Administration Route(s):
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):
Sample Package:
No
FDA Application Number:
M020
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
11-01-2024
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code 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 disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
72220-002-021 CONTAINER in 1 CARTON / 20 g in 1 CONTAINER (72220-002-01)

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 72220-002-04?

The NDC Packaged Code 72220-002-04 is assigned to a 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. The product's dosage form is stick and is administered via topical form.

Is NDC 72220-002 included in the NDC Directory?

Yes, Mdp Peptide 9 Bio Sun Pro with product code 72220-002 is active and included in the NDC Directory. The product was first marketed by Skinidea Co., Ltd on November 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 72220-002-04?

The 11-digit format is 72220000204. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-272220-002-045-4-272220-0002-04