NDC 62257-014 1014 Foaming Antimicrobial

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:
62257-014
Proprietary Name:
1014 Foaming Antimicrobial
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Abc Compounding Co., Inc.
Labeler Code:
62257
Start Marketing Date: [9]
05-01-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 62257-014-01

Package Description: 1200 mL in 1 CARTRIDGE

NDC Code 62257-014-03

Package Description: 350 mL in 1 CARTRIDGE

NDC Code 62257-014-05

Package Description: 540 mL in 1 BOTTLE, PLASTIC

NDC Code 62257-014-06

Package Description: 1 BAG in 1 BOX / 800 mL in 1 BAG

NDC Code 62257-014-07

Package Description: 700 mL in 1 BAG

NDC Code 62257-014-08

Package Description: 1 BAG in 1 BOX / 1000 mL in 1 BAG

NDC Code 62257-014-09

Package Description: 2000 mL in 1 CARTRIDGE

NDC Code 62257-014-10

Package Description: 1000 mL in 1 CARTRIDGE

NDC Code 62257-014-11

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC Code 62257-014-12

Package Description: 1000 mL in 1 BAG

NDC Code 62257-014-13

Package Description: 800 mL in 1 BAG

NDC Code 62257-014-14

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC Code 62257-014-15

Package Description: 946 mL in 1 BOTTLE, PLASTIC

NDC Code 62257-014-16

Package Description: 236 mL in 1 BOTTLE, PLASTIC

NDC Code 62257-014-17

Package Description: 532 mL in 1 BOTTLE, PLASTIC

NDC Code 62257-014-18

Package Description: 50 mL in 1 BOTTLE, PLASTIC

NDC Code 62257-014-24

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC Code 62257-014-27

Package Description: 800 mL in 1 CARTRIDGE

NDC Code 62257-014-28

Package Description: 149 mL in 1 BOTTLE, PLASTIC

NDC Code 62257-014-55

Package Description: 208200 mL in 1 DRUM

Product Details

What is NDC 62257-014?

The NDC code 62257-014 is assigned by the FDA to the product 1014 Foaming Antimicrobial which is product labeled by Abc Compounding Co., Inc.. The product's dosage form is . The product is distributed in 20 packages with assigned NDC codes 62257-014-01 1200 ml in 1 cartridge , 62257-014-03 350 ml in 1 cartridge , 62257-014-05 540 ml in 1 bottle, plastic , 62257-014-06 1 bag in 1 box / 800 ml in 1 bag, 62257-014-07 700 ml in 1 bag , 62257-014-08 1 bag in 1 box / 1000 ml in 1 bag, 62257-014-09 2000 ml in 1 cartridge , 62257-014-10 1000 ml in 1 cartridge , 62257-014-11 1000 ml in 1 bottle, plastic , 62257-014-12 1000 ml in 1 bag , 62257-014-13 800 ml in 1 bag , 62257-014-14 3785 ml in 1 bottle, plastic , 62257-014-15 946 ml in 1 bottle, plastic , 62257-014-16 236 ml in 1 bottle, plastic , 62257-014-17 532 ml in 1 bottle, plastic , 62257-014-18 50 ml in 1 bottle, plastic , 62257-014-24 118 ml in 1 bottle, plastic , 62257-014-27 800 ml in 1 cartridge , 62257-014-28 149 ml in 1 bottle, plastic , 62257-014-55 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 1014 Foaming Antimicrobial?

For hand-washing to decrease bacteria on the skin

Which are 1014 Foaming Antimicrobial UNII Codes?

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

Which are 1014 Foaming Antimicrobial 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:

* Please review the disclaimer below.

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".