Label: KETO-PLEX FORTE liquid

  • NDC Code(s): 50480-010-99
  • Packager: Radix Laboratories, Inc.
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated December 22, 2014

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  • CONTENTS (Per 1000ml):

    • Calcium Chloride Dihydrate ..................0.330g
    • Magnesium Chloride Hexahydrate .......0.260g
    • Total Protien ............................................2.7g
    • Dextrose H​2​O ......................................300.0g
    • Purified Water ..........................................q.s.
  • Inactives:

    • Sodium Chloride, Sodium
      Acetate, Potassium Acetate, Citric Acid,
      Methylparaben, Propylparaben
    • Contains the Following Amino Acids:
      L-Glutamic acid HCI, L-Arginine HCI,
      L-Proline, L-Lysine HCI, L-Leucine,
      L-Phenylalanine, L-Valine, L-Threonine,
      L-Isoleucine, L-Histidine HCI,
      L-Methionine, and L-Tyrosine
  • Indications:

    • An oral rehydration formula, containing a
      supplemental nutritive source of electrolytes,
      dextrose and amino acids for cattle, horse,
      sheep, goats and swine.
  • Storage:

    • Store at controlled room temperature between 59oF to 86oF (15oC -30oC).
  • Warnings:

    • Avoid storage at cold temperatures which can cause product to become cloudy.
    • To clarify place product in warm water bath (100oF-120oF) for about 30 minutes.
  • Dosage and administration:

    • Administer orally as a drench or by use of a stomach tube.
    • The usual recommended dose in adult cattle is 500mL to 1000mL depending on size and condition.
    • Can be repeated twice daily for 3 days.
  • Keep Away From Children

    • Keep away from children.
    • For animal use only.
  • Principal Display Panel

    Principal Display Panel

    Keto-Plex Forte Product Image

    1000 ml bottle

  • INGREDIENTS AND APPEARANCE
    KETO-PLEX FORTE 
    keto-plex forte liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:50480-010
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CHLORIDE0.330 g  in 1000 mL
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CHLORIDE0.260 g  in 1000 mL
    AMINO ACIDS (UNII: 0O72R8RF8A) (AMINO ACIDS - UNII:0O72R8RF8A) AMINO ACIDS2.7 g  in 1000 mL
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE300 g  in 1000 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50480-010-9912 in 1 CARTON
    11000 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/27/2013
    Labeler - Radix Laboratories, Inc. (108500091)
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