Label: V-MAX 50- virginiamycin powder

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

Drug Label Information

Updated November 7, 2023

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

  • DESCRIPTION

    To be mixed in cattle feed

  • Active Drug Ingredient

    Virginiamycin : 11%

    (Contains 50 g virginiamycin activity per lb)

    Caution

    CAUTION: Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

    Inert ingredients :

    Processed grain by-products, roughage products, calcium carbonate, carboxymethylcellulose, mineral oil

  • INDICATIONS & USAGE

    Important: Must be diluted in feed before use

    Follow Directions on Back Panel

    V-Max is a registered trademark of Phibro Animal Health Corporation

    Phibro Animal Health Corporation, Teaneck, NJ 07666

    Approved by FDA under NADA # 140-998

    8812000

    101-9141-06

    NET CONTENTS: 50 lb (22.7 kg)

    Distributed by:

    PHIBRO ANIMAL HEALTH, INC.

    Teaneck, NJ 07666, USA

  • (50 g virginiamycin activity per lb)For use in complete feeds for cattle fed in confinement for slaughter as specified belowDirections for Use

    Cattle fed in confinement for slaughter

    Virginiamycin required mg/hd/day

    Virginiamycin (g/tons) of complete feed (90% dry matter basis)

    Reduction of incidence of liver abscesse

    85–240

    13.5–16.0

    Caution: Not for use in animals intended for breeding.

  • Mixing Directions

    Preparation ofType B Medicated Feeds for cattle fed in confinement for slaughter—Thoroughly mix the following amounts of V-Max 50 Type A Medicated Article to make 1 ton of Type B Medicated Feed to provide the concentrations shown in Table 1. An intermediate blending step, consistent with the mixing equipment specifications, should be performed to ensure adequate mixing.

    Table 1. Type B Medicated Feed

    lb of V-Max 50 Type A Medicated Article per ton of supplement

    Virginiamycin concentration in Type B Medicated Feed (g/ton)

    5

    10

    20

    40

    100

    200

    250

    500

    1,000

    2,000

    5,000

    10,000

    Preparation of Type C Medicated Feed for cattle fed in confinement for slaughter:

    From Type B Medicated Feed: The Type B Medicated Feed must be diluted to a Type C Medicated Feed before being fed. Prepare a Type B Medicated Feed as described above. Thoroughly mix the V-Max 50 Type B Medicated Feed to make 1 ton of Type C Medicated Feed to provide 13.5 16.0 g of virginiamycin per ton of complete feed on a 90% dry matter basis using the examples provided in Table 2.

    Table 2. Type C Medicated Feed prepared from V-Max 50 Type B Medicated Feed

    lb of a 500g/ton Type B Medicated Feed per ton of complete feed

    lb of a 1,000 g/ton Type B Medicated Feed per ton of complete feed

    lb of a 5,000 g/ton Type B Medicated Feed per ton of complete feed

    lb of a 10,000 g/ton Type B Medicated Feed per ton of complete feed

    Virginiamycin concentration in complete feed 90% dry matter basis (g/ton)

    54

    27

    5.4

    2.7

    13.5

    64

    32

    6.4

    3.2

    16.0

    From Type A Medicated Article: V-Max 50 Type A Medicated Article must be diluted to a Type C Medicated Feed before being fed. Thoroughly mix the Type A Medicated Article to make 1 ton of Type C Medicated Feed to provide 13.5 – 16.0 g of virginiamycin per ton of complete feed on a 90% dry matter basis using the examples provided in Table 3.

    An intermediate blending step, consistent with the blending equipment specifications, should be performed to ensure adequate mixing.

    Table 3. Type C Medicated Feed prepared from V-Max 50 Type A Medicated Article

    lb of V-Max 50 Type A Medicated Article per ton of complete feed

    Virginiamycin concentration in complete feed 90% dry matter basis (g/ton)

    0.27

    0.32

    13.5

    16.0

    Feed continuously as sole ration

  • Store at or Below 25°C/77F°, Excursions Permitted Up To 40oC (104oF)

    Close container after use

  • INDICATIONS & USAGE

    NOT FOR HUMAN USE

    RESTRICTED DRUG (CALIFORNIA) – USE ONLY AS DIRECTED

  • V-Max 50

    V-Max 50 LabelV-Max 50

  • INGREDIENTS AND APPEARANCE
    V-MAX 50 
    virginiamycin powder
    Product Information
    Product TypeVFD TYPE A MEDICATED ARTICLE ANIMAL DRUGItem Code (Source)NDC:66104-9601
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VIRGINIAMYCIN (UNII: C49WS9N75L) (VIRGINIAMYCIN - UNII:C49WS9N75L) VIRGINIAMYCIN227 g  in 0.45 kg
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66104-9601-122.7 kg in 1 BAG
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NADANADA14099804/01/2010
    Labeler - Phibro Animal Health (006989008)
    Registrant - Phibro Animal Health (006989008)