Pro-tect Sunscreen For Professionals Lotion
NDC Package 37945-860-64

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

Pro-tect Sunscreen For Professionals (meradimate, octinoxate, octisalate, oxybenzone) lotions is •Apply this product topically to affected areas and allow to dry without rubbing. This formulation utilizes a lotion delivery system. Marketed by Bio-medical & Pharmaceutical Manufacturing Corporation, this product is identified by NDC 37945-860 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
37945-860-64
Package Description
100 g in 1 CONTAINER
Product Code
37945-860
11-Digit Billing Format
37945086064

Clinical Specifications

Proprietary Name
Pro-tect Sunscreen For Professionals
Non-Proprietary Name
Meradimate, Octinoxate, Octisalate, Oxybenzone
Substance Name
Meradimate; Octinoxate; Octisalate; Oxybenzone
Dosage Form
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
Administration Route
Cutaneous - Administration to the skin.
Active Ingredient(s)
Usage Information
•Apply this product topically to affected areas and allow to dry without rubbing. •Use up to 3 times daily. •Use only as directed.

Regulatory & Marketing

Labeler Name
Bio-medical & Pharmaceutical Manufacturing Corporation
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-01-1980
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 (37945-860). Click a package code to view its specific billing and regulatory data.

37945-860-50
1880 g in 1 CONTAINER
37945-860-65
190 g in 1 CONTAINER

* 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 37945-860-64 identifies a specific commercial package of 100 g in 1 container of Pro-tect Sunscreen For Professionals, a human over the counter drug labeled by Bio-medical & Pharmaceutical Manufacturing Corporation. This lotion is formulated for cutaneous use and contains meradimate; octinoxate; octisalate; oxybenzone 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 Bio-medical & Pharmaceutical Manufacturing Corporation on November 01, 1980. The current certification is valid through December 31, 2026.

How is this Bio-medical & Pharmaceutical Manufacturing Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 37945086064. 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)
37945-860-64
11-Digit CMS (5-4-2)
37945-0860-64

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