Label: SPEC-TUSS- guaifenesin powder

  • NDC Code(s): 59051-8867-4
  • Packager: Neogen Corporation-Mercer
  • 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 November 1, 2018

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

  • DESCRIPTION

    Spec-tuss

    Palatable Expectorant Powder

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  • USE IN SPECIFIC POPULATIONS

    FOR ANIMAL USE ONLY

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  • COMPONENTS

    Each ounce (28.4 g) contains:
    Guaifenesin USP................................2 g (7% w/w)

    In a base of sucrose, potassium iodide, ammonium chloride, artificial coloring and flavoring.

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  • Indications:

    A palatable powder used as an expectorant in horses.

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  • WARNING:

    KEEP OUT OF REACH OF CHILDREN

    Warning:

    For horses only. Not for human use. Do not use in lactating mares.

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  • Dosage and Administration:

    1 teaspoon per 250 lb body weight orally in feed or via dose syringe.

    Adult Horses:Not to exceed 1/2 oz twice daily or as directed by your veterinarian.

    Foals and Ponies: Consult your veterinarian.

    For best results, horse should receive medication for 3-4 days.

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  • STORAGE AND HANDLING

    Store in a cool, dry place.

    Keep container tightly closed.

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  • SPL UNCLASSIFIED SECTION

    Lot No.

    Exp. Date:

    Manufactured by: Neogen Corporation, Lexington, KY 40511

    859-254-1221 • animalsafety.neogen.com   L103-0918

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  • SPL UNCLASSIFIED SECTION

    Made in the USA

    Item No. 08867

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  • PRINCIPAL DISPLAY PANEL - 1 lb

    NDC: 59051-8867-4

    Spec-tuss

    Palatable Expectorant Powder

    NEOGEN® Vet

    Net Contents: 1 lb (454 g)

    Spec-Tuss

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  • INGREDIENTS AND APPEARANCE
    SPEC-TUSS 
    guaifenesin powder
    Product Information
    Product Type OTC ANIMAL DRUG Item Code (Source) NDC:59051-8867
    Route of Administration Oral
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 70.4 mg  in 1 g
    Product Characteristics
    Color      Score     
    Shape Size
    Flavor VANILLA Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:59051-8867-4 454 g in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 07/22/2013
    Labeler - Neogen Corporation-Mercer (042125879)
    Establishment
    Name Address ID/FEI Business Operations
    Neogen Corporation-Mercer 042125879 analysis, label, manufacture
    Establishment
    Name Address ID/FEI Business Operations
    Zhejiang Haizhou Pharmaceutical Co., Ltd 530737642 api manufacture
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