Animal NDC 51437-108-08 Nootie Medicated Pet

Chlorhexidine Gluconate, Ketoconazole

Animal Product Information

Field Name Field Value
Animal NDC Code 51437-108-08
Proprietary Name Nootie Medicated Pet 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 Chlorhexidine Gluconate, Ketoconazole 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 Nootie Llc
Product Type Otc Animal Drug
Usage Information
    Use on dry skin. Spray directly on the affected area or over the entire body, avoiding the face and ears. Massage into the skin until absorbed. Do not allow animal to lick treated area until dry to prevent ingestion. If spraying the entire body, brush coat once dry. Wash hands after use. For best results, use once daily or as directed by veterinarian.
Active Ingredient(s)
  • Ketoconazole
  • Chlorhexidine Gluconate
Inactive Ingredient(s)
  • WATER (059QF0KO0R)
  • GLYCERIN (PDC6A3C0OX)
  • PROPYLENE GLYCOL (6DC9Q167V3)
  • POLYSORBATE 20 (7T1F30V5YH)
  • LACTIC ACID, UNSPECIFIED FORM (33X04XA5AT)
  • ALOE VERA LEAF (ZY81Z83H0X)
  • PEG-75 LANOLIN (09179OX7TB)
  • SODIUM LACTATE (TU7HW0W0QT)
  • METHYLISOTHIAZOLINONE (229D0E1QFA)
  • WATER (059QF0KO0R)
  • GLYCERIN (PDC6A3C0OX)
  • PROPYLENE GLYCOL (6DC9Q167V3)
  • POLYSORBATE 20 (7T1F30V5YH)
  • LACTIC ACID, UNSPECIFIED FORM (33X04XA5AT)
  • ALOE VERA LEAF (ZY81Z83H0X)
  • PEG-75 LANOLIN (09179OX7TB)
  • SODIUM LACTATE (TU7HW0W0QT)
  • METHYLISOTHIAZOLINONE (229D0E1QFA)
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.

Nootie Medicated Pet Images

Nootie Medicated Pet 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



Drug Facts




Active Ingredients:



Chlorhexidine Gluconate 2%
Ketoconazole 1%


Other Ingredients:



Purified Water, Glycerin, Propylene Glycol, Polysorbate 20, Lactic Acid, Aloe Barbadensis (Aloe Vera) Leaf Juice, PEG-75 Lanolin, Sodium Lactate, Fragrance, Methylisothiazolinone.


Uses:



For topical skin conditions responsive to Chlorhexidine Gluconate and Ketoconazole.


Warnings:



 For animal use only.
 For topical use on dogs and cats.
 Avoid contact with eyes and mucous membranes.
 If eye contact occurs or skin irritation develops, rinse thoroughly with water, discontinue use and immediately consult your veterinarian.
Keep out of reach of children.


Directions:



Use on dry skin. Spray directly on the affected area or over the entire body, avoiding the face and ears. Massage into the skin until absorbed. Do not allow animal to lick treated area until dry to prevent ingestion. If spraying the entire body, brush coat once dry. Wash hands after use. For best results, use once daily or as directed by veterinarian.


Storage:



Store at room temperature (60 - 80°F). Protect from high temperatures. Protect from freezing.


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