NDC 65133-170 Aire-master Foaming Ab Handsoap

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:
65133-170
Proprietary Name:
Aire-master Foaming Ab Handsoap
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
65133
Start Marketing Date: [9]
01-01-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 65133-170?

The NDC code 65133-170 is assigned by the FDA to the product Aire-master Foaming Ab Handsoap which is product labeled by Aire-master Of America, Inc.. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 65133-170-02 208198 ml in 1 drum , 65133-170-03 946353 ml in 1 container , 65133-170-09 4 bottle, plastic in 1 case / 3785 ml in 1 bottle, plastic (65133-170-01), 65133-170-10 24 bottle in 1 case / 237 ml in 1 bottle (65133-170-04), 65133-170-11 12 bottle in 1 case / 532 ml in 1 bottle (65133-170-05), 65133-170-12 8 pouch in 1 package / 1000 ml in 1 pouch (65133-170-06), 65133-170-13 48 bottle in 1 case / 50 ml in 1 bottle (65133-170-07). 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 Aire-master Foaming Ab Handsoap?

Uses  Handwash to help reduce bacteria that potentially can cause disease

Which are Aire-master Foaming Ab Handsoap UNII Codes?

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

Which are Aire-master Foaming Ab Handsoap 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:

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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".