Label: VITAMIN AD- retinol cholecalciferol injection

  • NDC Code(s): 13985-332-02, 13985-332-04, 13985-332-05
  • Packager: MWI Veterinary Supply, Inc.
  • 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 April 18, 2019

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

View All Sections
  • INDICATIONS & USAGE

    Sterile Solution

    For Animal Use Only
    Keep Out of Reach of Children

    INDICATIONS

    For use as a supplemental nutritive source of vitamins A and D in cattle.

  • CAUTION

    Do not inject into meat animals within 60 days of marketing. 

    Administration of this product to well nourished animals may cause hypervitaminosis D which may result in hypercalcemia.  This condition may be harmful to the animal.

  • DOSAGE AND ADMINISTRATION

    Inject intramuscularly or subcutaneously preferably  in the neck area using aseptic technique.

    Calves- 1/2 to 1 mL,
    Yearling Cattle- 1 to 2 mL
    Adult Cattle- 2 to 4 mL

    These suggested dosage may be repeated after 60 days, if necessary.

  • COMPONENTS

    Each mL of sterile solution contains:

    ACTIVE INGREDIENTS

    Vitamin A  . . . . . . . . . 500,000 IU
    Vitamin D3  . . . . . . . . . 75,000 IU

    INACTIVE INGREDIENTS

    In an emulsifiable base with vitamin E (antioxidant), N-methylpyrrolidone, polyoxyethylated (30) castor oil, propylene glycol dicaprylate, polyoxyethylene (20) sorbitan monooleate and benzyl alcohol 2%.

  • STORAGE

    Store at controlled room temperature between 15o and 30oC (59-86oF).

    PROTECT FROM LIGHT AND EXCESSIVE HEAT.

    TAKE TIME OBSERVE LABEL DIRECTIONS

  • PRINCIPAL DISPLAY PANEL

    V1 Vit AD

  • INGREDIENTS AND APPEARANCE
    VITAMIN AD 
    retinol cholecalciferol injection
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:13985-332
    Route of AdministrationINTRAMUSCULAR, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RETINOL (UNII: G2SH0XKK91) (RETINOL - UNII:G2SH0XKK91) RETINOL500000 [iU]  in 1 mL
    CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41) CHOLECALCIFEROL75000 [iU]  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13985-332-02100 mL in 1 VIAL
    2NDC:13985-332-05250 mL in 1 VIAL
    3NDC:13985-332-04500 mL in 1 VIAL
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/30/2012
    Labeler - MWI Veterinary Supply, Inc. (019926120)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events (Animal Drug), FDA Safety Recalls (Animal Drug)

Related Resources

Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!