Label: VETERICYN TRIPLE ACTION EAR TREATMENT- hydrocortisone liquid

  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 6, 2024

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  • Active Ingredient

    Hydrocortisone

  • Description

    Vetericyn® Ear Treatment is intended for use in removing debris and alleviating itch caused by irritation and inflammation for otitis externa (i.e., outer ear infection).

  • Dosage/Administration

    Shake well. Fill ear canal with product and gently massage the affected area, allowing it to stay inside ear. Wipe away excess liquid. Head shaking after application is common. Repeat once (1) per day for seven (7)days. Consult your veterinarian for extended use.

  • Warning

    Animal use only, not for humans. Keep out of reach of children. Avoid contact with eyes. If condition does not improve after seven (7) days or if irritation or systemic condition develop, stop use and contact your veterinarian. Do not use in conjunction with other ear solutions. Do not use on ruptured ear drum. Avoid water near ears during treatment.

  • Inactive Ingredient

    Benzoic Acid, Benzyl Alcohol, Buffer, Chrysanthemum Indicum Flower Extract, Dehydroacetic Acid, Glycerin,Hydroxypropyl Cellulose, Lysozyme, Phellodendron Chinense Bark Extract, Propylene Glycol, Sorbic Acid, Water.

  •  Precautions

    Store at room temperature. Do not use after expiration date. Cap applicator tip after use. Follow general guidelines for safe medication disposal.

  • Questions

    vetericyn.com | 866.318.3116

  • Product label

    image descriptionimage description

  • INGREDIENTS AND APPEARANCE
    VETERICYN TRIPLE ACTION EAR TREATMENT 
    hydrocortisone liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:70489-1023
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    SORBIC ACID (UNII: X045WJ989B)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    CHRYSANTHEMUM INDICUM FLOWER (UNII: I6OER6U04L)  
    HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
    WATER (UNII: 059QF0KO0R)  
    LYSOZYME (UNII: 968JKA7T33)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    PHELLODENDRON CHINENSE WHOLE (UNII: QKA3ZK8IIE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70489-1023-11 in 1 CARTON
    144 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/01/2024
    Labeler - INNOVACYN INC. (025217003)
    Establishment
    NameAddressID/FEIBusiness Operations
    Westwood Laboratories, LLC.832280635api manufacture
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