Label: NICARB- nicarbazin powder

  • Category: OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Animal Drug Application

Drug Label Information

Updated November 6, 2023

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

  • INDICATIONS & USAGE

    As an aid in preventing outbreaks of cecal (Eimeria tenella) and intestinal (E. acervulina, E. maxima, E. necatrix,and E. brunetti) coccidiosis in chickens.

  • ACTIVE DRUG INGREDIENT

    Nicarbazin . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25%

    INGREDIENTS

    Wheat Middlings, Soybean Oil and Microtracer

  • MIXING DIRECTIONS

    NICARB (nicarbazin) 25% should be thoroughly and evenly mixed in the feed in accordance with current good manufacturing practice for feed. Type C medicated feeds should contain 0.01 – 0.02% nicarbazin. Uniformly mix 0.8 – 1.6 pounds of Nicarb 25% with one of the feed ingredients to make at least 10 pounds of premix before final mixing. Mix the resulting premix with feed to make 1 ton (2000 lb) of finished feed containing 0.01 – 0.02% nicarbazin.

    SUGGESTED DIRECTIONS FOR FEED TAGS

    Use Directions

    Use Nicarbazin Type C medicated feed as the only ration from the time chicks are placed on litter until past the time when coccidiosis is ordinarily a hazard.

  • CAUTION:

    Do not feed to laying chickens.

    Do not use as a treatment for outbreaks of coccidiosis. Do not use in flushing mashes.

    If losses exceed 0.5 percent in a 2-day period, obtain an accurate diagnosis and follow the instructions of your veterinarian or poultry pathologist.

    Broilers fed feed medicated with NICARB 25% may show reduced heat tolerance when exposed to high temperature and high humidity to which they have not been accustomed and under severe conditions, fatalities may result. An ample supply of drinking water and adequate ventilation will improve the birds’ tolerance of heat.

  • WARNING:

    Withdraw 4 days before slaughter when used at levels ≤ 0.0125%.

    Withdraw 5 days before slaughter when used at levels >0.0125%

    Keep this and all drugs out of the reach of children.

    NOT FOR HUMAN USE

    RESTRICTED DRUG (CALIFORNIA) – USE ONLY AS DIRECTED

  • SPL UNCLASSIFIED SECTION

    SEE DIRECTIONS ON BACK PANEL

    Net Wt 50 lb (22.68 kg)

    8205000

    101-9018-13

    Approved by FDA under NADA  #009-476

    NICARB REG TM Phibro Animal Health Corporation

    MICROTRACER REG TM Micro-Tracers, Inc. San Francisco, CA

    Generic Section

    Distributed by:

    Phibro Animal Health Corporation, Teaneck, NJ 07666

  • Nicarb 25 Label

    Nicarb LabelNicarb 25 Label

  • INGREDIENTS AND APPEARANCE
    NICARB 
    nicarbazin powder
    Product Information
    Product TypeOTC TYPE A MEDICATED ARTICLE ANIMAL DRUGItem Code (Source)NDC:66104-8200
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NICARBAZIN (UNII: 11P9NUA12U) (4,4'-DINITROCARBANILIDE - UNII:9IDD210E75) NICARBAZIN113.4 g  in 0.45 kg
    Inactive Ingredients
    Ingredient NameStrength
    SOYBEAN OIL (UNII: 241ATL177A)  
    WHEAT MIDDLINGS (UNII: 12H8QE0WQI)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66104-8200-022.68 kg in 1 BAG
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NADANADA00947607/08/2009
    Labeler - Phibro Animal Health (006989008)
    Registrant - Phibro Animal Health (006989008)