Animal NDC 17030-002-01 Clotrimazole

Animal Product Information

Field Name Field Value
Animal NDC Code 17030-002-01
Proprietary Name Clotrimazole 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 Clotrimazole 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 Vetoquinol Usa, Inc.
Product Type Otc Animal Drug
Usage Information
    Clean and dry affected area. Apply a thin layer morning and evening or as directed by veterinarian. If satisfactory results are not obtained within 2 weeks, consult your veterinarian.
Active Ingredient(s)
  • Clotrimazole
Inactive Ingredient(s)
  • PROPYLENE GLYCOL (6DC9Q167V3)
  • ALCOHOL (3K9958V90M)
  • CHLOROXYLENOL (0F32U78V2Q)
  • COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (H2KVQ74JM4)
  • PHOSPHATE ION (NK08V8K8HR)
  • BENZYL ALCOHOL (LKG8494WBH)
  • CITRIC ACID MONOHYDRATE (2968PHW8QP)
  • SODIUM HYDROXIDE (55X04QC32I)
  • PROPYLENE GLYCOL (6DC9Q167V3)
  • ALCOHOL (3K9958V90M)
  • CHLOROXYLENOL (0F32U78V2Q)
  • COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (H2KVQ74JM4)
  • PHOSPHATE ION (NK08V8K8HR)
  • BENZYL ALCOHOL (LKG8494WBH)
  • CITRIC ACID MONOHYDRATE (2968PHW8QP)
  • SODIUM HYDROXIDE (55X04QC32I)
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.

Clotrimazole 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



Other



Drug Facts

Active Ingredient

Clotrimazole, USP 1%

Purpose

Antifungal

411417 7


Uses



For dermatological conditions responsive to Clotrimazole.


Warnings



For external use only. Not for internal use.


When Using This Product



  • Avoid contact with eyes or mucous membranes. If contact occurs, immediately flush with water.

Stop Use And Consult Your Veterinarian If



  • Skin irritation occurs.

Safe Handling Warning



Keep out of reach of children.


Directions



Clean and dry affected area. Apply a thin layer morning and evening or as directed by veterinarian. If satisfactory results are not obtained within 2 weeks, consult your veterinarian.


Other Information



  • Store at controlled room temperature (15-30° C)
  • See bottom for Lot No. and Expiration Date.

Inactive Ingredients



Propylene Glycol, SD Alcohol 40B, Chloroxylenol, Cocamidopropyl PG-Dimonium Chloride Phosphate, Benzoyl Alcohol, Citric Acid (pH adjustment), Sodium Hydroxide (pH adjustment).


Questions?



Manufactured for:
Vetoquinol USA, Inc.
Ft. Worth, TX (USA) 76137
www.vetoquinolusa.com
1 (800) 267-5707


Principal Display Panel - 30 Ml Bottle Label



NDC 17030-002-01

Clotrimazole Solution

1% CLOTRIMAZOLE

DROPS FOR
DOGS & CATS

Net Contents: 1 fl oz (30 mL)

vetoquinoL


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