Label: NOOTIE HEXZOLE MEDICATED PET FLUSH- chlorhexidine gluconate, ketoconazole solution
- NDC Code(s): 51437-107-08
- 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.
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients:
- Other Ingredients:
- Uses:
- Warnings:
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Directions:
For use on ears, apply solution to the ear canal and with firm but gentle pressure, massage the base of the ear. Use an absorbent material to clean any excess solution. For topical skin use, apply solution to the affected area and use a cotton ball to absorb any excess solution. Wash hands after application. Use once daily or as directed by your veterinarian.
- Storage:
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SPL UNCLASSIFIED SECTION
Nootie™ DERMATOLOGY SOLUTIONS
TOPICAL EAR & SKIN TREATMENT
HELPS TREAT AND RELIEVE:
› Hot Spots
› Ringworm
› Allergic Dermatitis
› Topical Ear & Skin ConditionsFOR DOGS AND CATS
√ Formulated with veterinarian strength active ingredients.
√ Helps treat and manage ear and skin conditions responsive to Chlorhexidine and Ketoconazole.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
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INGREDIENTS AND APPEARANCE
NOOTIE HEXZOLE MEDICATED PET FLUSH
chlorhexidine gluconate, ketoconazole solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:51437-107 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE 2 mg in 1 mL KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I) KETOCONAZOLE 2 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) NONOXYNOL-12 (UNII: 6NR43D77O6) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) POLYSORBATE 20 (UNII: 7T1F30V5YH) LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT) BENZYL ALCOHOL (UNII: LKG8494WBH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51437-107-08 237 mL in 1 BOTTLE 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)