Zinc Oxide, Titanium Dioxide
NDC Package 70798-415-22

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Zinc Oxide, Titanium Dioxide is useshelps prevent sunburnhigher SPF gives more sunburn protectionWarningsFor external use onlyDo not use on damaged or broken skin. Marketed by Matchco Inc., this product is identified by NDC 70798-415 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
70798-415-22
Package Description
30 g in 1 BOTTLE, GLASS
Product Code
11-Digit Billing Format
70798041522

Clinical Specifications

Proprietary Name
Zinc Oxide, Titanium Dioxide
Dosage Form
-
Usage Information
Useshelps prevent sunburnhigher SPF gives more sunburn protectionWarningsFor external use onlyDo not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Regulatory & Marketing

Labeler Name
Matchco Inc.
FDA Application #
part352
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
07-11-2016
Listing Expiration
12-31-2017
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 70798-415-22 identifies a specific commercial package of 30 g in 1 bottle, glass of Zinc Oxide, Titanium Dioxide, labeled by Matchco Inc.. 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 Matchco Inc. on July 11, 2016. The current certification is valid through December 31, 2017.

How is this Matchco Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70798041522. 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)
70798-415-22
11-Digit CMS (5-4-2)
70798-0415-22

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