Sun Bum Face 50 Premium Sunscreen Spf 50 Lotion
NDC Package 44717-080-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Sun Bum Face 50 Premium Sunscreen Spf 50 (avobenzone, homosalte, octisalate, octocrylene) lotions is stop use and ask a doctor if rash occurs. This formulation utilizes a lotion delivery system. Marketed by Wasatch Product Development, Llc, this product is identified by NDC 44717-080 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
44717-080-01
Package Description
88 mL in 1 TUBE
Product Code
11-Digit Billing Format
44717008001

Clinical Specifications

Proprietary Name
Sun Bum Face 50 Premium Sunscreen Spf 50
Non-Proprietary Name
Avobenzone, Homosalte, Octisalate, Octocrylene
Substance Name
Avobenzone; Homosalate; Octisalate; Octocrylene
Dosage Form
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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.
Usage Information
Stop use and ask a doctor if rash occurs.

Regulatory & Marketing

Labeler Name
Wasatch Product Development, Llc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-01-2023
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy 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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 44717-080-01 identifies a specific commercial package of 88 ml in 1 tube of Sun Bum Face 50 Premium Sunscreen Spf 50, a human over the counter drug labeled by Wasatch Product Development, Llc. This lotion is formulated for topical use and contains avobenzone; homosalate; octisalate; octocrylene 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 Wasatch Product Development, Llc on February 01, 2023. The current certification is valid through December 31, 2026.

How is this Wasatch Product Development, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 44717008001. 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)
44717-080-01
11-Digit CMS (5-4-2)
44717-0080-01

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