Dermaroller Anhydrous Sunscreen Cream
NDC Package 59958-201-01

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

Package Information

Dermaroller Anhydrous Sunscreen (titanium dioxide, zinc oxide) cream is directionsApply evenly before sun exposure and as needed.  For children under 6 months of age: aska doctor.  Reapply as needed or after toweldrying, swimming or perspiring. This formulation utilizes a cream delivery system. Marketed by Owen Biosciences, Inc., this product is identified by NDC 59958-201 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
59958-201-01
Package Description
30 g in 1 TUBE
Product Code
59958-201
11-Digit Billing Format
59958020101

Clinical Specifications

Proprietary Name
Dermaroller Anhydrous Sunscreen Spf 30
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.
Active Ingredient(s)
Usage Information
DirectionsApply evenly before sun exposure and as needed.  For children under 6 months of age: aska doctor.  Reapply as needed or after toweldrying, swimming or perspiring.

Regulatory & Marketing

Labeler Name
Owen Biosciences, Inc.
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-01-2011
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 59958-201-01 identifies a specific commercial package of 30 g in 1 tube of Dermaroller Anhydrous Sunscreen Spf 30, a human over the counter drug labeled by Owen Biosciences, Inc.. 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 Owen Biosciences, Inc. on March 01, 2011. The current certification is valid through December 31, 2026.

How is this Owen Biosciences, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 59958020101. 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)
59958-201-01
11-Digit CMS (5-4-2)
59958-0201-01

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