Sunof Sunscreen Spf 50
NDC Package 77418-003-01

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Sunof Sunscreen Spf 50 is shake well. Marketed by Atak Farma Kozmetik Ve Kimya Sanayi Ticaret Anonim Sirketi, this product is identified by NDC 77418-003 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
77418-003-01
Package Description
200 mL in 1 BOTTLE, DISPENSING
Product Code
77418-003
11-Digit Billing Format
77418000301

Clinical Specifications

Proprietary Name
Sunof Sunscreen Spf 50
Dosage Form
-
Usage Information
Shake well . Hold container 4 or 6 inches from the skin to apply. Spray liberally and spread evenly by hand 15 minutes before sun exposure. Do not spray directly into face. Spray on hands and then apply to face. Do not apply in windy conditions. Use in a well-ventilated area.Reapply : after 80 minutes of swimming or sweating.Immediately after towel drying. At least every 2 hours . Children under 6 months : Ask a doctor. Sun Protection Measures . Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk , regularly use a sunscreen with a board spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun , especially from 10 a.m. – 2 p.m. wear long-sleeved shirts, pants,hats and sunglasses.

Regulatory & Marketing

Labeler Name
Atak Farma Kozmetik Ve Kimya Sanayi Ticaret Anonim Sirketi
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-05-2025
End Marketing Date
01-05-2025
Listing Expiration
01-05-2025
Exclude Flag
D
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 77418-003-01 identifies a specific commercial package of 200 ml in 1 bottle, dispensing of Sunof Sunscreen Spf 50, labeled by Atak Farma Kozmetik Ve Kimya Sanayi Ticaret Anonim Sirketi. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Atak Farma Kozmetik Ve Kimya Sanayi Ticaret Anonim Sirketi on January 05, 2025. The current certification is valid through January 05, 2025.

How is this Atak Farma Kozmetik Ve Kimya Sanayi Ticaret Anonim Sirketi product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 77418000301. 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)
77418-003-01
11-Digit CMS (5-4-2)
77418-0003-01

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