Surface Sun Dry Touch Spf 70 Sunscreen
NDC Package 72344-005-06

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 inactivated by the FDA.

Surface Sun Dry Touch Spf 70 Sunscreen is spray liberally and evenly by hand 15 minutes before sun exposure.Reapply after:80 minutes of sweating or swimming immediately after towel drying at least every 2 hours Hold can 4-6 inches from the skin to apply. Marketed by Surface Products Corp, this product is identified by NDC 72344-005 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
72344-005-06
Package Description
170 mL in 1 CAN
Product Code
72344-005
11-Digit Billing Format
72344000506

Clinical Specifications

Proprietary Name
Surface Sun Dry Touch Spf 70 Sunscreen
Dosage Form
-
Usage Information
Spray liberally and evenly by hand 15 minutes before sun exposure.Reapply after:80 minutes of sweating or swimming immediately after towel drying at least every 2 hours Hold can 4-6 inches from the skin to apply. Do not spray directly into your face. Spray on hands an then apply to face. Do not apply in windy conditions. Use in a well-ventilated area.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 broad spectrum SPF 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. Children under 6 months: ask a doctor.

Regulatory & Marketing

Labeler Name
Surface Products Corp
FDA Application #
part352
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
03-14-2018
Listing Expiration
12-31-2019
Exclude Flag
I
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 72344-005-06 identifies a specific commercial package of 170 ml in 1 can of Surface Sun Dry Touch Spf 70 Sunscreen, labeled by Surface Products Corp. 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 Surface Products Corp on March 14, 2018. The current certification is valid through December 31, 2019.

How is this Surface Products Corp product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72344000506. 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)
72344-005-06
11-Digit CMS (5-4-2)
72344-0005-06

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