Publix
NDC Package 56062-709-16

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 is     apply literally 15 minutes before sun exposure    reapply: after 80 minutes of swimming or sweating    immediately after towel drying    at least every 2 hoursSun protection measures.Spending time in the sun increase your risk of skin cancer and early skin aging. Marketed by Publix Super Markets Inc, this product is identified by NDC 56062-709 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
56062-709-16
Package Description
226 g in 1 BOTTLE, PLASTIC
Product Code
56062-709
11-Digit Billing Format
56062070916

Clinical Specifications

Proprietary Name
Publix Spf 30
Dosage Form
-
Usage Information
    apply literally 15 minutes before sun exposure    reapply: after 80 minutes of swimming or sweating    immediately after towel drying    at least every 2 hoursSun protection measures.Spending time in the sun increase 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 am - 2 pm    Wear long sleeves shirts, pants, hats and sunglasses    children under 6 month of age: Ask a doctor

Regulatory & Marketing

Labeler Name
Publix Super Markets Inc
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
07-16-2013
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 56062-709-16 identifies a specific commercial package of 226 g in 1 bottle, plastic of Publix Spf 30, labeled by Publix Super Markets 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 Publix Super Markets Inc on July 16, 2013. The current certification is valid through December 31, 2019.

How is this Publix Super Markets Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 56062070916. 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)
56062-709-16
11-Digit CMS (5-4-2)
56062-0709-16

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