Sodium Sufide
NDC Package 0363-9560-85

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.

Sodium Sufide is adults and children 12 yers and over:wash affected area and dry thoroghlyplace retainer ring on toe with slot over the area where the ingrown nail and the skin meet. Marketed by Walgreens Company, this product is identified by NDC 0363-9560 and is authorized under FDA application part358D.

Identification & Billing

NDC Package Code
0363-9560-85
Package Description
8.5 g in 1 PACKAGE
Product Code
0363-9560
11-Digit Billing Format
00363956085
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sodium Sufide
Dosage Form
-
Usage Information
Adults and children 12 yers and over:wash affected area and dry thoroghlyplace retainer ring on toe with slot over the area where the ingrown nail and the skin meet. Smooth ring down firmlycut open tip of the tube on score mark. Apply enough gel prodcut to fill the slot in the ring. Immeciately replace cap on tubeplace round center section of bandage directly over the gel- filled ring to seal the gel in place. Smooth ends of bandage strips around toerepeat twice daily (morning and night) for up to 7 days until pain discomfort is relieved or until the nail can be lifted out of the nail groove and easliy trimmedChildren under 12 years: ask a doctor

Regulatory & Marketing

Labeler Name
Walgreens Company
FDA Application #
part358D
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
03-01-2018
Listing Expiration
12-31-2021
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 0363-9560-85 identifies a specific commercial package of 8.5 g in 1 package of Sodium Sufide, labeled by Walgreens Company. 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 Walgreens Company on March 01, 2018. The current certification is valid through December 31, 2021.

How is this Walgreens Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00363956085. 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 (4-4-2)
0363-9560-85
11-Digit CMS (5-4-2)
00363-9560-85

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