NDC 52559-576 Anchor Foaming Mango

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:
52559-576
Proprietary Name:
Anchor Foaming Mango
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
52559
Start Marketing Date: [9]
04-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 52559-576?

The NDC code 52559-576 is assigned by the FDA to the product Anchor Foaming Mango which is product labeled by Anchor Supply Company. The product's dosage form is . The product is distributed in 20 packages with assigned NDC codes 52559-576-01 1200 ml in 1 cartridge , 52559-576-03 350 ml in 1 cartridge , 52559-576-05 540 ml in 1 bottle, plastic , 52559-576-06 1 bag in 1 box / 800 ml in 1 bag, 52559-576-07 700 ml in 1 bag , 52559-576-08 1 bag in 1 box / 1000 ml in 1 bag, 52559-576-09 2000 ml in 1 cartridge , 52559-576-10 1000 ml in 1 cartridge , 52559-576-11 1000 ml in 1 bottle, plastic , 52559-576-12 1000 ml in 1 bag , 52559-576-13 800 ml in 1 bag , 52559-576-14 3785 ml in 1 bottle, plastic , 52559-576-15 946 ml in 1 bottle, plastic , 52559-576-16 236 ml in 1 bottle, plastic , 52559-576-17 532 ml in 1 bottle, plastic , 52559-576-18 50 ml in 1 bottle, plastic , 52559-576-24 118 ml in 1 bottle, plastic , 52559-576-27 800 ml in 1 cartridge , 52559-576-28 149 ml in 1 bottle, plastic , 52559-576-55 208200 ml in 1 drum . 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 Anchor Foaming Mango?

For hand-washing to decrease bacteria on the skin

Which are Anchor Foaming Mango UNII Codes?

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

Which are Anchor Foaming Mango 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 Anchor Foaming Mango?

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".