Ultimate Sheer Spf 55 Body
NDC Package 36800-722-04

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.

Ultimate Sheer Spf 55 Body is • spray liberally and spread evenly by hand 15 minutes before sun exposure• reapply: • after 80 minutes of swimming or sweating• immediately after towel drying • at least every 2 hours• hold container 4 to 6 inches from the skin to apply • do not spray directlyinto face. Marketed by Topco, this product is identified by NDC 36800-722 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
36800-722-04
Package Description
141 g in 1 CAN
Product Code
36800-722
11-Digit Billing Format
36800072204

Clinical Specifications

Proprietary Name
Ultimate Sheer Spf 55 Body
Dosage Form
-
Usage Information
• spray liberally and spread evenly by hand 15 minutes before sun exposure• reapply: • after 80 minutes of swimming or sweating• immediately after towel drying • at least every 2 hours• hold container 4 to 6 inches from the skin to apply • do not spray directlyinto face. Spray on hands then apply to face. • do not apply in windyconditions • use in a well-ventilated area• Sun Protection Measures. Spending time in the sun increases your risk ofskin cancer and early skin aging. To decrease this risk, regularly use asunscreen with a broad spectrum SPF of 15 or higher and other sunprotection measures including: • limit time in the sun, especially from10 a.m. – 2 p.m. • wear long-sleeve shirts, pants, hats, and sunglasses• children under 6 months: Ask a doctor

Regulatory & Marketing

Labeler Name
Topco
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
12-13-2012
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 36800-722-04 identifies a specific commercial package of 141 g in 1 can of Ultimate Sheer Spf 55 Body, labeled by Topco. 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 Topco on December 13, 2012. The current certification is valid through December 31, 2019.

How is this Topco product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 36800072204. 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)
36800-722-04
11-Digit CMS (5-4-2)
36800-0722-04

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