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  4. NDC Product Code: 0363-9560 Sodium Sufide

NDC 0363-9560 Sodium Sufide

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 0363-9560?
  4. Sodium Sufide Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0363-9560
Proprietary Name:
Sodium Sufide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walgreens Company
Labeler Code:
0363
Product Label ID:
5e081d6c-0619-4d6c-be50-588c488404eb
Start Marketing Date: [9]
03-01-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 0363-9560-85

Package Description: 8.5 g in 1 PACKAGE

Product Details

What is NDC 0363-9560?

The NDC code 0363-9560 is assigned by the FDA to the product Sodium Sufide which is product labeled by Walgreens Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-9560-85 8.5 g in 1 package . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Sodium Sufide?

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

Which are Sodium Sufide UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Sodium Sufide Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Sodium Sufide?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".