NDC 69530-856 Cln Acne Cleanser

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:
69530-856
Proprietary Name:
Cln Acne Cleanser
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
69530
Start Marketing Date: [9]
03-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69530-856?

The NDC code 69530-856 is assigned by the FDA to the product Cln Acne Cleanser which is product labeled by Topmd Skin Care. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69530-856-44 1 bottle, plastic in 1 carton / 75 ml in 1 bottle, plastic, 69530-856-45 1 bottle, plastic in 1 carton / 75 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 Cln Acne Cleanser?

Cleanse twice daily or as indicated by your physicianTreat whole areaWet the skinDispense into wet handsMassage area gently for 30 seconds working to create a latherRinse thoroughly with warm waterIf bothersome dryness or peeling occurs, reduce use to once a day or every other day.

Which are Cln Acne Cleanser UNII Codes?

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

Which are Cln Acne Cleanser 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 Cln Acne Cleanser?

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".