Label: NEOPLEX- neomycin sulfate powder

  • NDC Code(s): 55999-069-13, 55999-069-15, 55999-069-18, 55999-069-56, view more
    55999-069-57
  • Packager: Seachem Laboratories Inc.
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated July 16, 2018

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  • VETERINARY INDICATIONS

    NeoPlex™ is a broad spectrum antibiotic effective against most external infections of both marine and freshwater fish. Used as directed, NeoPlex™ will not discolor the water or damage the filter bed. It is well tolerated by invertebrates, although delicate species may be stressed.

  • DOSAGE & ADMINISTRATION

    DIRECTIONS: Use 1 level measure (included) to every 8 L (2 US gallons). Repeat every 7 days for up to 3 weeks or until symptoms disappear. Do not use UV, ozone, or chemical filtration during use. Remove with carbon before turning on UV.

  • SPL UNCLASSIFIED SECTION

    Active ingredients: neomycin sulfate (43%)

    Inactive ingredients: excipients (57%)

  • SAFE HANDLING WARNING

    For use in ornamental aquariums only. Not for human consumption.

  • SPL UNCLASSIFIED SECTION

    Seachem Laboratories Inc. • 1000 Seachem Drive, Madison, GA 30650

    www.seachem.com • support@seachem.com

  • PRINCIPAL DISPLAY PANEL - 10 g Vial Carton

    NeoPlex™

    EXTERNAL
    FUNGAL &
    BACTERIAL
    DISEASE

    Broad Spectrum Antibiotic Effective
    Against Most External Infections

    Marine & Freshwater

    Net Contents: 10 g (0.35 oz)

    Seachem®

    PRINCIPAL DISPLAY PANEL - 10 g Vial Carton
  • INGREDIENTS AND APPEARANCE
    NEOPLEX 
    neomycin sulfate powder
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:55999-069
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Neomycin Sulfate (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) Neomycin Sulfate425 mg  in 1 g
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55999-069-566 in 1 CASE
    1NDC:55999-069-571 in 1 CARTON
    1NDC:55999-069-1310 g in 1 VIAL, PLASTIC
    2NDC:55999-069-15100 g in 1 VIAL, PLASTIC
    3NDC:55999-069-181000 g in 1 VIAL, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Unapproved drug other01/01/1985
    Labeler - Seachem Laboratories Inc. (133041806)
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