NDC 71315-100 Aplaus Hand And Skin Sanitizer

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:
71315-100
Proprietary Name:
Aplaus Hand And Skin Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Katan Technologies Usa, Llc
Labeler Code:
71315
Start Marketing Date: [9]
05-01-2017
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Product Packages

NDC Code 71315-100-01

Package Description: 10 mL in 1 BOTTLE, SPRAY

NDC Code 71315-100-08

Package Description: 80 mL in 1 BOTTLE, SPRAY

NDC Code 71315-100-22

Package Description: 220 mL in 1 BOTTLE, SPRAY

NDC Code 71315-100-38

Package Description: 3780 mL in 1 JUG

NDC Code 71315-100-50

Package Description: 50 mL in 1 BOTTLE, SPRAY

NDC Code 71315-100-55

Package Description: 550 mL in 1 BOTTLE, PUMP

NDC Code 71315-100-60

Package Description: 60 mL in 1 BOTTLE, SPRAY

NDC Code 71315-100-99

Package Description: 1000 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 71315-100?

The NDC code 71315-100 is assigned by the FDA to the product Aplaus Hand And Skin Sanitizer which is product labeled by Katan Technologies Usa, Llc. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 71315-100-01 10 ml in 1 bottle, spray , 71315-100-08 80 ml in 1 bottle, spray , 71315-100-22 220 ml in 1 bottle, spray , 71315-100-38 3780 ml in 1 jug , 71315-100-50 50 ml in 1 bottle, spray , 71315-100-55 550 ml in 1 bottle, pump , 71315-100-60 60 ml in 1 bottle, spray , 71315-100-99 1000 ml in 1 bottle, spray . 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 Aplaus Hand And Skin Sanitizer?

For hand and skin sanitizing to decrease microbes on skin Recommended for repeated use

Which are Aplaus Hand And Skin Sanitizer UNII Codes?

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

Which are Aplaus Hand And Skin Sanitizer 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 Aplaus Hand And Skin Sanitizer?

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".