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  4. NDC Product Code: 62032-111 Clenziderm Daily Care Foaming Cleanser Acne Treatment

NDC 62032-111 Clenziderm Daily Care Foaming Cleanser Acne Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62032-111?
  4. Clenziderm Daily Care Foaming Cleanser Acne Treatment 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:
62032-111
Proprietary Name:
Clenziderm Daily Care Foaming Cleanser Acne Treatment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Omp, Inc.
Labeler Code:
62032
Product Label ID:
934ec314-1ab7-45ee-a2fe-8bff3ff981b6
Start Marketing Date: [9]
02-01-2007
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 62032-111?

The NDC code 62032-111 is assigned by the FDA to the product Clenziderm Daily Care Foaming Cleanser Acne Treatment which is product labeled by Omp, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62032-111-60 118 ml in 1 bottle, plastic . 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 Clenziderm Daily Care Foaming Cleanser Acne Treatment?

Use AM and PMwet facegently massage product all over face for 20–30 seconds avoiding eye arearinse thoroughly and pat drywait 10–15 minutes to allow skin to dry completely. cleanse the skin thoroughly before applying medicationcover the entire affected area with a thin layer one to three times dailybecause excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctorif bothersome dryness or peeling occurs, reduce application to once a day or every other day. clean the skin thoroughly before applying this productcover the entire affected area with a thin layer one to three times dailybecause excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctorif bothersome dryness or peeling occurs, reduce application to once a day or every other dayif going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

Which are Clenziderm Daily Care Foaming Cleanser Acne Treatment UNII Codes?

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

Which are Clenziderm Daily Care Foaming Cleanser Acne Treatment 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 Clenziderm Daily Care Foaming Cleanser Acne Treatment?

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".