Drs. Pharmacy Sunscreen Spf 30 (physical Filters) Cream
NDC Package 80489-887-01

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

Drs. Pharmacy Sunscreen Spf 30 (physical Filters) (sunscreen spf 30) cream is a medication used as Sunscreen Agent. This formulation utilizes a cream delivery system. Marketed by Ol Pharma Tech Llc. (drs. Pharmacy), this product is identified by NDC 80489-887 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
80489-887-01
Package Description
133 g in 1 TUBE
Product Code
80489-887
11-Digit Billing Format
80489088701

Clinical Specifications

Proprietary Name
Drs. Pharmacy Sunscreen Spf 30 (physical Filters)
Non-Proprietary Name
Sunscreen Spf 30
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
This product is used as Sunscreen Agent. • 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
Ol Pharma Tech Llc. (drs. Pharmacy)
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-01-2024
Listing Expiration
12-31-2027
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 (80489-887). Click a package code to view its specific billing and regulatory data.

80489-887-02
118 g in 1 TUBE
80489-887-03
85 g in 1 TUBE

* 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 80489-887-01 identifies a specific commercial package of 133 g in 1 tube of Drs. Pharmacy Sunscreen Spf 30 (physical Filters), a human over the counter drug labeled by Ol Pharma Tech Llc. (drs. Pharmacy). 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 Ol Pharma Tech Llc. (drs. Pharmacy) on January 01, 2024. The current certification is valid through December 31, 2027.

How is this Ol Pharma Tech Llc. (drs. Pharmacy) product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 80489088701. 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)
80489-887-01
11-Digit CMS (5-4-2)
80489-0887-01

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