Degil Sun Spf 50 Sunscreen Lotion
NDC Package 58331-075-01

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

Package Information

Degil Sun Spf 50 Sunscreen (homosalate, octisalate, oxybenzone, avobenzone, octocrylene) lotions is sun Protection Factor 50 • SPF 50 • Helps prevent sunburn • Sunburn protectant• Helps protect from sunburn • If used as directed with other sun protection measures [see Directions (for Use)], decreases the risk of skin cancer and early skin aging caused by the sun • Water Resistant (80 minutes). This formulation utilizes a lotion delivery system. Marketed by Degil Safety Products (1989) Inc, this product is identified by NDC 58331-075 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
58331-075-01
Package Description
120 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
58331007501

Clinical Specifications

Proprietary Name
Degil Sun Spf 50 Sunscreen
Non-Proprietary Name
Homosalate, Octisalate, Oxybenzone, Avobenzone, Octocrylene
Substance Name
Avobenzone; Homosalate; Octisalate; Octocrylene; Oxybenzone
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
Sun Protection Factor 50 • SPF 50 • Helps prevent sunburn • Sunburn protectant• Helps protect from sunburn • If used as directed with other sun protection measures [see Directions (for Use)], decreases the risk of skin cancer and early skin aging caused by the sun • Water Resistant (80 minutes)

Regulatory & Marketing

Labeler Name
Degil Safety Products (1989) Inc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-01-2024
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (58331-075). Click a package code to view its specific billing and regulatory data.

750 mL in 1 BOTTLE

* 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 58331-075-01 identifies a specific commercial package of 120 ml in 1 bottle of Degil Sun Spf 50 Sunscreen, a human over the counter drug labeled by Degil Safety Products (1989) Inc. This lotion is formulated for topical use and contains avobenzone; homosalate; octisalate; octocrylene; 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 Degil Safety Products (1989) Inc on May 01, 2024. The current certification is valid through December 31, 2026.

How is this Degil Safety Products (1989) Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 58331007501. 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)
58331-075-01
11-Digit CMS (5-4-2)
58331-0075-01

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