Sul-Q-Nox: Product Information

SUL-Q-NOX- sulfaquinoxaline solution
Huvepharma, Inc

Sul-Q-Nox®

31.92% (Sulfaquinoxaline as sodium and potassium salts)

ANTIMICROBIAL

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.)

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

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.

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).

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

INDICATIONS DOSAGE 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, repeattreatment at this level for 2 more days.CAUTION: Do not change litter unless absolutelynecessary. Do not give flushing mashes.
COCCIDIOSIS — TURKEYS: Control of coccidiosis caused by Eimeria meleagrimitis, E. adenoeides , susceptible tosulfaquinoxaline. 13 fl. oz. (0.025%) Give for 2 days — skip 3 days — give for 2 days — skip 3 daysand give 2 more days. Repeat if necessary.CAUTION: Do not change litter unless absolutelynecessary. Do not give flushing mashes.
ACUTE FOWL CHOLERA — CHICKENS AND TURKEYS: Control of acute fowl cholera caused byPasteurella multocida susceptible tosulfaquinoxaline.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 diseaserecurs, repeat treatment. Poultry that have survived fowltyphoid outbreaks should not be kept for laying housereplacements or breeders unless tests show they are notcarriers.
COCCIDIOSIS — CATTLE AND CALVES: For the control and treatment of coccidiosiscaused by Eimeria bovis , E. zuernii , susceptibleto sulfaquinoxaline. 7¾ fl. oz. (0.015%) 6 mg/lb of body wt.

Give for 3-5 days. As a generalization, cattle and calveswill consume approx. 1 gal/100 lbs body weight/day. Cattleor 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.

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SUL-Q-NOX sulfaquinoxaline solution
Product Information
Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:23243-6771
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SULFAQUINOXALINE (SULFAQUINOXALINE) SULFAQUINOXALINE .3192 g in 1 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:23243-6771-2 4 PACKAGE in 1 BOX contains a PACKAGE
1 3785 mL in 1 PACKAGE This package is contained within the BOX (23243-6771-2)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NADA NADA006891 07/09/2019
Labeler — Huvepharma, Inc (619153559)
Registrant — Huvepharma EOOD (552671651)
Establishment
Name Address ID/FEI Operations
Huvepharma, Inc 883128204 analysis, label, manufacture, pack

Revised: 10/2023 Huvepharma, Inc

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