Label: FUNGUS FIGHTER- phenol liquid

  • NDC Code(s): 49794-017-28, 49794-017-32
  • Packager: Continental Manufacturing Chemist, Inc.
  • 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 March 22, 2011

If you are a consumer or patient please visit this version.

  • Indications:

    For use on Cattle, Sheep, Horses, Dogs and other large animals as an aid in the control of ringworm, summer itch, girth itch, foot rot and other fungal infections.  Do not use on cats.

  • Directions for use:

    Shake well.  Clean the area to be treated, and apply Fungus Fighter directly to the affected area, soaking completely.  Let dry.  Repeat application daily until condition improves, up to 4 consecutive days.  For Foot Rot, apply directly to the affected area, soaking completely.  Use daily until condition improves.

  • Precautions:

    Use only as directed.  For external animal use only. KEEP OUT OF REACH OF CHILDREN.  Avoid contact with eyes and mucous membranes.  If irritation develops, or if condition does not improve, discontinue use and consult veterinarian.  Not intended for use on animals in commercial food production.

  • Warning:

    Flammable!Keep away from excessive heat or open flame.

  • Inactive Ingredients:

    Ethyl Alcohol, o-Phenylphenol, Polyvinylprrolidone, Propylene Glycol, Purified Water

  • INGREDIENTS AND APPEARANCE
    FUNGUS FIGHTER 
    phenol liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:49794-017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    phenol (UNII: 339NCG44TV) (Phenol - UNII:339NCG44TV) phenol0.50 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    alcohol (UNII: 3K9958V90M)  
    propylene glycol (UNII: 6DC9Q167V3)  
    water (UNII: 059QF0KO0R)  
    ORTHOPHENYLPHENOL (UNII: D343Z75HT8)  
    POVIDONE K30 (UNII: U725QWY32X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49794-017-32946 mL in 1 BOTTLE, PLASTIC
    2NDC:49794-017-283785 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/12/2010
    Labeler - Continental Manufacturing Chemist, Inc. (005278007)
    Establishment
    NameAddressID/FEIBusiness Operations
    Continental Manufacturing Chemist, Inc.005278007manufacture