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  4. NDC Product Code: 42582-500 Sulfacetamide Sodium And Sulfur

NDC 42582-500 Sulfacetamide Sodium And Sulfur

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 42582-500?
  4. Sulfacetamide Sodium And Sulfur Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
42582-500
Proprietary Name:
Sulfacetamide Sodium And Sulfur
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bi-coastal Pharma International Llc
Labeler Code:
42582
Product Label ID:
5f633aac-6f6a-467a-8047-9b5f1929d00b
Start Marketing Date: [9]
06-01-2011
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 42582-500?

The NDC code 42582-500 is assigned by the FDA to the product Sulfacetamide Sodium And Sulfur which is product labeled by Bi-coastal Pharma International Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42582-500-21 1 bottle in 1 carton / 454 g in 1 bottle. 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 Sulfacetamide Sodium And Sulfur?

Sulfacetamide sodium and sulfur wash is indicated in the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.

Which are Sulfacetamide Sodium And Sulfur UNII Codes?

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

Which are Sulfacetamide Sodium And Sulfur 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:

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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".