Animal NDC 17307-3641-4 Xtra Blu Part B
Sodium Chlorite Solution

Animal Product Information

Field Name Field Value
Animal NDC Code 17307-3641-4
Proprietary Name Xtra Blu Part B What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Sodium Chlorite Solution 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.
Labeler Name Agrochem Inc
Product Type Otc Animal Drug
Active Ingredient(s)
  • Sodium Chlorite
Inactive Ingredient(s)
  • WATER (059QF0KO0R)
  • WATER (059QF0KO0R)
Marketing Category UNAPPROVED DRUG OTHER 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.

Xtra Blu Part B Images

Xtra Blu Part B Animal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Xtra Blu (Part B)



XTRA BLU  (PART B)

SPRAY

DIP CUP

FOAM


* The information on this page is for an ANIMAL PRODUCT, please review the complete disclaimer below.