Label: SUL-Q-NOX- sulfaquinoxaline solution

  • Category: PRESCRIPTION ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Animal Drug Application

Drug Label Information

Updated October 5, 2023

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

  • SPL UNCLASSIFIED SECTION

    Sul-Q-Nox®

    31.92% (Sulfaquinoxaline as sodium and potassium salts)

    ANTIMICROBIAL

  • PRECAUTIONS

    Caution: Federal (USA) law restricts this drug to use by or on the
    order of a licensed veterinarian.
    For Use in Animal Drinking Water Only
    Sulfonamide

    KEEP OUT OF REACH OF CHILDREN
    KEEP TIGHTLY SEALED WHEN NOT IN USE

    Restricted Drug (California) - Use only as directed. Not for human use.

    Net Contents: 1 Gallon (128 fl. oz.)

  • SPL UNCLASSIFIED SECTION

    Manufactured for:
    Huvepharma, Inc.
    525 Westpark Drive, Suite 230
    Peachtree City, GA 30269

    HUVEPHARMA®

    HUVEPHARMA and Sul-Q-Nox are registered
    trademarks of Huvepharma EOOD

    Take Time

    Approved by FDA under NADA # 006-891
    P08-4001SL
    Rev. 01-2022

  • GENERAL PRECAUTIONS

    CAUTION:

    • May cause toxic reactions unless drug is evenly mixed in water at dosages indicated and used according
    to directions.
    • Levels of sulfaquinoxaline higher than 0.025% in feed or 0.012% in water for more than 24 to 36 hours
    may result in reduced growth rate in chickens as a result of reduced feed or water intake.
    • For control of disease outbreaks, medication should be initiated as soon as diagnosis is determined.
    • Treated animals must actually consume enough medicated water to provide a necessary dosage of
    approximately 10 to 45 mg/lb/day in chickens and 3.5 to 55 mg/lb/day in turkeys and 6 mg/lb/day in
    cattle and calves, depending on class of animal, ambient temperature, age, and other factors.
    • Prolonged administration of sulfaquinoxaline at higher doses may result in depressed feed or water
    intake, deposition of sulfaquinoxaline crystals in kidney and interference with normal blood clotting.
    • Do not mix or administer in galvanized containers.
    • The follwing word is required on this product to comply with Agricultural Code of California:
    HAZARDOUS
    • CAUSES SKIN AND EYE BURNS. Avoid contact with eyes, skin, or clothing. In case of contact, flush
    immediately with water for at least 15 minutes; for eye get medical attention.

  • WARNINGS

    WARNING:

    • Withdraw use of product 10 days before slaughter.
    • A withdrawal period has not been established for this product in pre-ruminating
    calves. Do not use in calves to be processed for veal.
    • Do not medicate chickens or turkeys producing eggs for human
    consumption.
    • Not for use in lactating dairy cattle.
    • DISPOSE OF ANY WASTE OR UNUSED PORTION PROPERLY.
    • KEEP ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.
    • Store between 20°- 25°C (68°- 77°F); excursions permitted between
    15°- 40°C (59°- 104°F).

  • INDICATIONS & USAGE

    FOR AUTOMATIC DRINKING WATER PROPORTIONERS
    FOR CONTROL OR TREATMENT OF THE FOLLOWING DISEASES WHEN CAUSED BY ONE
    OR MORE PATHOGENIC ORGANISMS SUSCEPTIBLE TO SULFAQUINOXALINE
    PREPARE MEDICATED DRINKING WATER FRESH DAILY

                   INDICATIONSDOSAGE PER 128 GALLONS OF
    WATER
                                     TREATMENT
    COCCIDIOSIS — CHICKENS:
    Control of coccidiosis caused by Eimeria tenella,
    E. necatrix, E. maxima, E. brunetti, E. acervulina,
    susceptible to sulfaquinoxaline. 
    20½ fl. oz.
    (0.04%)

                Give for 2-3 days, skip 3 days.

                                              Then

    13 fl. oz.
    (0.025%)
    Give for 2 days more. If bloody droppings appear, repeat
    treatment at this level for 2 more days.
    CAUTION: Do not change litter unless absolutely
    necessary. Do not give flushing mashes.
    COCCIDIOSIS — TURKEYS:
    Control of coccidiosis caused by Eimeria
    meleagrimitis, E. adenoeides, susceptible to
    sulfaquinoxaline.
    13 fl. oz.
    (0.025%)
    Give for 2 days - skip 3 days - give for 2 days - skip 3 days
    and give 2 more days. Repeat if necessary.
    CAUTION: Do not change litter unless absolutely
    necessary. Do not give flushing mashes.
    ACUTE FOWL CHOLERA — CHICKENS AND
    TURKEYS:
    Control of acute fowl cholera caused by
    Pasteurella multocida susceptible to
    sulfaquinoxaline.
    FOWL TYPHOID — CHICKENS AND TURKEYS:
    Control of fowl typhoid caused by Salmonella
    gallinarum, susceptible to sulfaquinoxaline.
    20½ fl. oz.
    (0.04%)
    Use for 2-3 days. Move birds to clean ground. If disease
    recurs, repeat treatment. Poultry that have survived fowl
    typhoid outbreaks should not be kept for laying house
    replacements or breeders unless tests show they are not
    carriers.
    COCCIDIOSIS — CATTLE AND CALVES:
    For the control and treatment of coccidiosis
    caused by Eimeria bovis, E. zuernii, susceptible
    to sulfaquinoxaline.
    7¾ fl. oz.
    (0.015%)
    6 mg/lb
    of body wt.

    Give for 3-5 days. As a generalization, cattle and calves
    will consume approx. 1 gal/100 lbs body weight/day. Cattle
    or calves not eating or drinking must be treated

    individually.

    To report suspected adverse drug events, for technical assistance or to obtain a copy of the Safety Data Sheet (SDS), contact Huvepharma, Inc. at 1-877-994-4883 or www.huvepharma.us. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or http://www.fda.gov/reportanimalae.

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    SUL-Q-NOX 
    sulfaquinoxaline solution
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:23243-6771
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFAQUINOXALINE (UNII: WNW8115TM9) (SULFAQUINOXALINE - UNII:WNW8115TM9) SULFAQUINOXALINE.3192 g  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:23243-6771-24 in 1 BOX
    13785 mL in 1 PACKAGE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NADANADA00689107/09/2019
    Labeler - Huvepharma, Inc (619153559)
    Registrant - Huvepharma EOOD (552671651)
    Establishment
    NameAddressID/FEIBusiness Operations
    Huvepharma, Inc883128204analysis, label, manufacture, pack