NDC 19339-020 Esco Fresh Pure Hand

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:
19339-020
Proprietary Name:
Esco Fresh Pure Hand
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Arca Inc.
Labeler Code:
19339
Start Marketing Date: [9]
03-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 19339-020-02

Package Description: 20 POUCH in 1 CARTON / 35 mL in 1 POUCH (19339-020-01)

NDC Code 19339-020-03

Package Description: 500 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 19339-020?

The NDC code 19339-020 is assigned by the FDA to the product Esco Fresh Pure Hand which is product labeled by Arca Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 19339-020-02 20 pouch in 1 carton / 35 ml in 1 pouch (19339-020-01), 19339-020-03 500 ml in 1 bottle, pump . 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 Esco Fresh Pure Hand?

Directions:Take an appropriate amount on your hands and rub thoroughly to dry.

Which are Esco Fresh Pure Hand UNII Codes?

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

Which are Esco Fresh Pure Hand 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 Esco Fresh Pure Hand?

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".