NDC 42546-145 Pr Benzoyl Peroxide Wash

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:
42546-145
Proprietary Name:
Pr Benzoyl Peroxide Wash
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prugen, Inc.
Labeler Code:
42546
Start Marketing Date: [9]
10-26-2009
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 42546-145-16

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

Price per Unit: $0.15661 per ML

Product Details

What is NDC 42546-145?

The NDC code 42546-145 is assigned by the FDA to the product Pr Benzoyl Peroxide Wash 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 42546-145-16 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 Pr Benzoyl Peroxide Wash?

INDICATIONS AND USAGE:PRTM Benzoyl Peroxide Wash is indicated for the topical treatment of acne vulgaris.

Which are Pr Benzoyl Peroxide Wash UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Pr Benzoyl Peroxide Wash?

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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Patient Education

Benzoyl Peroxide Topical


Benzoyl peroxide is used to treat mild to moderate acne.
[Learn More]


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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".