NOOTIE MEDICATED PET- chlorhexidine gluconate, ketoconazole spray

Nootie Medicated Pet by

Drug Labeling and Warnings

Nootie Medicated Pet by is a Animal medication manufactured, distributed, or labeled by Nootie LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

SPL UNCLASSIFIED SECTION

Nootie™ DERMATOLOGY SOLUTIONS

TOPICAL SKIN TREATMENT

HELPS TREAT AND RELIEVE:
› Hot Spots
› Ringworm
› Skin Infections
› Allergic Dermatitis
› Topical Skin Conditions

FOR DOGS AND CATS

√ Formulated with veterinarian strength active ingredients.
√ Helps treat and manage skin conditions responsive to Chlorhexidine and Ketoconazole.
√ For best results, use with Nootie Medicated Shampoo.

MADE IN USA

Manufactured for and distributed by Nootie LLC
6421 Congress Ave., Suite 121, Boca Raton, FL 33487
1-800-478-7713  Nootie.com

Packaging

INGREDIENTS AND APPEARANCE

NOOTIE MEDICATED PET 
chlorhexidine gluconate, ketoconazole spray

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 51437-108
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	20 mg  in 1 mL
KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I)	KETOCONAZOLE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PEG-75 LANOLIN (UNII: 09179OX7TB)
SODIUM LACTATE (UNII: TU7HW0W0QT)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51437-108-08	237 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/24/2022

Labeler - Nootie LLC (008995795)