NDC 24415-201 Aluminum Chlorohydrate

Solution - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.
NDC Product Code:
24415-201
Proprietary Name:
Aluminum Chlorohydrate
Non-Proprietary Name: [1]
Aluminum Chlorohydrate
Substance Name: [2]
Aluminum Chlorohydrate
NDC Directory Status:
Bulk Ingredient
Product Type: [3]
UNFINISHED PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Labeler Name: [5]
Gulbrandsen Technologies Inc
Labeler Code:
24415
Marketing Category: [8]
BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
Start Marketing Date: [9]
01-01-2006
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Unfinished Product: [13]
Yes
Code Navigator:

Product Packages

NDC Code 24415-201-01

Package Description: 208 kg in 1 DRUM

NDC Code 24415-201-02

Package Description: 1041 kg in 1 CONTAINER

NDC Code 24415-201-03

Package Description: 1249 kg in 1 CONTAINER

NDC Code 24415-201-04

Package Description: 19000 kg in 1 BAG

NDC Code 24415-201-05

Package Description: 22500 kg in 1 BAG

NDC Code 24415-201-06

Package Description: 23000 kg in 1 BAG

NDC Code 24415-201-07

Package Description: 24000 kg in 1 BAG

NDC Code 24415-201-08

Package Description: 272 kg in 1 DRUM

NDC Code 24415-201-09

Package Description: 275 kg in 1 DRUM

NDC Code 24415-201-10

Package Description: 1340 kg in 1 CONTAINER

NDC Code 24415-201-11

Package Description: 1350 kg in 1 CONTAINER

NDC Code 24415-201-12

Package Description: 1360 kg in 1 CONTAINER

NDC Code 24415-201-13

Package Description: 20000 kg in 1 CONTAINER

NDC Code 24415-201-14

Package Description: 22000 kg in 1 CONTAINER

NDC Code 24415-201-15

Package Description: 19050 kg in 1 CONTAINER

Product Details

What is NDC 24415-201?

The NDC code 24415-201 is assigned by the FDA to the UNFINISHED product Aluminum Chlorohydrate which is a bulk ingredient product labeled by Gulbrandsen Technologies Inc. The generic name of Aluminum Chlorohydrate is aluminum chlorohydrate. The product's dosage form is solution. The product is distributed in 15 packages with assigned NDC codes 24415-201-01 208 kg in 1 drum , 24415-201-02 1041 kg in 1 container , 24415-201-03 1249 kg in 1 container , 24415-201-04 19000 kg in 1 bag , 24415-201-05 22500 kg in 1 bag , 24415-201-06 23000 kg in 1 bag , 24415-201-07 24000 kg in 1 bag , 24415-201-08 272 kg in 1 drum , 24415-201-09 275 kg in 1 drum , 24415-201-10 1340 kg in 1 container , 24415-201-11 1350 kg in 1 container , 24415-201-12 1360 kg in 1 container , 24415-201-13 20000 kg in 1 container , 24415-201-14 22000 kg in 1 container , 24415-201-15 19050 kg in 1 container . 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 Aluminum Chlorohydrate Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

* Please review the disclaimer below.

Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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".

[13] What is an Unfinished Product? - This field indicates if the product is an unfinished drug. An unfinished drug is an active pharmaceutical ingredient either alone or with other ingredients that is not a finished drug product. Unfinished drugs are used to process other drugs or for drug compounding.