NDC 42546-175 Sulfacleanse 8/4

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
42546-175
Proprietary Name:
Sulfacleanse 8/4
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prugen, Inc.
Labeler Code:
42546
Start Marketing Date: [9]
05-01-2011
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)

Product Packages

NDC Code 42546-175-16

Package Description: 1 BOTTLE, PUMP in 1 BOX / 473 mL in 1 BOTTLE, PUMP

Price per Unit: $0.21083 per ML

Product Details

What is NDC 42546-175?

The NDC code 42546-175 is assigned by the FDA to the product Sulfacleanse 8/4 which is product labeled by Prugen, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42546-175-16 1 bottle, pump in 1 box / 473 ml in 1 bottle, pump. 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 Sulfacleanse 8/4?

SulfaCleanse® 8/4 (sodium sulfacetamide 8% & sulfur 4%) is indicated for the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.

Which are Sulfacleanse 8/4 UNII Codes?

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

Which are Sulfacleanse 8/4 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 Sulfacleanse 8/4?

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:
  • RxCUI: 1010234 - sulfacetamide sodium 8 % / sulfur 4 % Medicated Liquid Soap
  • RxCUI: 1010234 - sulfacetamide sodium 80 MG/ML / sulfur 40 MG/ML Medicated Liquid Soap
  • RxCUI: 1010234 - sulfacetamide sodium 8 % / sulfur 4 % Topical Suspension

* Please review the disclaimer below.

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".