Matte Tinted Mineral Sunscreen Cream
NDC Package 85642-203-15

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

Matte Tinted Mineral Sunscreen (titanium dioxide, zinc oxide) cream is a human otc drug administered via topical route. This formulation utilizes a cream delivery system. Marketed by Edit Eurospa, Llc, this product is identified by NDC 85642-203 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
85642-203-15
Package Description
1.5 g in 1 PACKET
Product Code
85642-203
11-Digit Billing Format
85642020315

Clinical Specifications

Proprietary Name
Matte Tinted Mineral Sunscreen
Non-Proprietary Name
Titanium Dioxide, Zinc Oxide
Substance Name
Titanium Dioxide; Zinc Oxide
Dosage Form
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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.
  • 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)

Regulatory & Marketing

Labeler Name
Edit Eurospa, Llc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-21-2023
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
Yes

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 (85642-203). Click a package code to view its specific billing and regulatory data.

85642-203-50
53 g in 1 BOTTLE, PUMP

* 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 85642-203-15 identifies a specific commercial package of 1.5 g in 1 packet of Matte Tinted Mineral Sunscreen, a human over the counter drug labeled by Edit Eurospa, Llc. This cream is formulated for topical use and contains titanium dioxide; zinc oxide 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 Edit Eurospa, Llc on March 21, 2023. The current certification is valid through December 31, 2026.

How is this Edit Eurospa, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85642020315. 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)
85642-203-15
11-Digit CMS (5-4-2)
85642-0203-15

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