Animal NDC 48106-2039-1 Arctic Blu Plus
Heptanoic Acid

Animal Product Information

Field Name Field Value
Animal NDC Code 48106-2039-1
Proprietary Name Arctic Blu Plus 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 Heptanoic Acid 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 Boumatic, Llc
Product Type Otc Animal Drug
Usage Information
    NOT FOR HUMAN USEFOR EXTERNAL USE ONLYUSE AT FULL STRENGTHFIRST AID:If in eyes: Hold eye open and rinse slowly and gently with water for 15-20 minutes. Remove contact lenses,if present after the first 5 minutes, then continue rinsing. Contact a physician immediately. If swallowed:Have person sip a glass of water if able to swallow. Do not give anything to an unconscious person. Do notinduce vomiting. Contact a physician immediately. If breathing difficulty occurs: Move person to fresh air.Contact a physician immediately. If on skin: Take off contaminated clothing. Rinse skin with soap and water.If irritation develops and persists, contact a physician.Have the product container or label with you when going for treatment, calling a physician, the emergencynumber listed on this label or MSDS, or a poison control center.
Active Ingredient(s)
  • Propylene Glycol
  • Glycerin
  • Heptanoic Acid
Inactive Ingredient(s)
  • C8-10/PROPYLENE GLYCOL/PEG-22/DECYLENE GLYCOL ETHER (F8S8XRX18H)
  • WATER (059QF0KO0R)
  • C8-10/PROPYLENE GLYCOL/PEG-22/DECYLENE GLYCOL ETHER (F8S8XRX18H)
  • 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.

Arctic Blu Plus Images

Arctic Blu Plus 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



Use Directions



NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
USE AT FULL STRENGTH

FIRST AID:
If in eyes: Hold eye open and rinse slowly and gently with water for 15-20 minutes. Remove contact lenses,
if present after the first 5 minutes, then continue rinsing. Contact a physician immediately. If swallowed:
Have person sip a glass of water if able to swallow. Do not give anything to an unconscious person. Do not
induce vomiting. Contact a physician immediately. If breathing difficulty occurs: Move person to fresh air.
Contact a physician immediately. If on skin: Take off contaminated clothing. Rinse skin with soap and water.
If irritation develops and persists, contact a physician.
Have the product container or label with you when going for treatment, calling a physician, the emergency
number listed on this label or MSDS, or a poison control center.


Storage:



Store in a closed container away from sources of heat. If product becomes frozen, thaw and mix
well before use.


Post Dipping



Dip as much of the
surface of each teat as possible immediately
after milking.
Note: If solution in cup becomes visibly
dirty, replenish with a fresh mixture
of this product. Do not return
unused product to original container.


Arctic Blu Plus Label



Arctic Blu Plus label


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