Publix Ultra Dish Detergent Orange
NDC Package 63691-032-10

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.

Publix Ultra Dish Detergent Orange is wet hands and forearms. Marketed by Sun Products Corporation, this product is identified by NDC 63691-032 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
63691-032-10
Package Description
709 mL in 1 BOTTLE, PLASTIC
Product Code
63691-032
11-Digit Billing Format
63691003210

Clinical Specifications

Proprietary Name
Publix Ultra Dish Detergent Orange
Dosage Form
-
Usage Information
Wet hands and forearms. Apply 5 ml or palmful to hands and forearms. Scrub thoroughly for 30 sec. and rinse.

Regulatory & Marketing

Labeler Name
Sun Products Corporation
FDA Application #
part333E
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
04-30-2016
Listing Expiration
12-31-2018
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 63691-032-10 identifies a specific commercial package of 709 ml in 1 bottle, plastic of Publix Ultra Dish Detergent Orange, labeled by Sun Products Corporation. 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 Sun Products Corporation on April 30, 2016. The current certification is valid through December 31, 2018.

How is this Sun Products Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63691003210. 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)
63691-032-10
11-Digit CMS (5-4-2)
63691-0032-10

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