Label: NOOTIE MEDICATED PET- chlorhexidine gluconate, ketoconazole spray
- NDC Code(s): 51437-108-08
- Packager: Nootie LLC
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated November 24, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients:
- Other Ingredients:
- Uses:
- Warnings:
-
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:
-
SPL UNCLASSIFIED SECTION
Nootie™ DERMATOLOGY SOLUTIONS
TOPICAL SKIN TREATMENT
HELPS TREAT AND RELIEVE:
› Hot Spots
› Ringworm
› Skin Infections
› Allergic Dermatitis
› Topical Skin ConditionsFOR 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 sprayProduct 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)