Label: DEXPANTHENOL injection, solution

  • Category: PRESCRIPTION ANIMAL DRUG LABEL

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 1, 2008

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  • DESCRIPTION

    NDC 54925-064-10

    DEXPANTHENOL INJECTION

    Net Contents: 100 mL

    FOR ANIMAL USE ONLY
    KEEP OUT OF REACH OF CHILDREN

    CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

    Rev. 4/08
    MED-PHARMEX
    INCORPORATED
    Pomona, CA 91767

  • INDICATIONS & USAGE

    COMPOSITION: Each mL contains:
    Dexpanthenol………………………………..250 mg
    Benzyl Alcohol…………………………...…1% w/v
    Water for Injection……………….…………….. q.s.
    Acetic Acid, Glacial, USP………….. to adjust pH

    INDICATIONS: For use as a nutritional source of dexpanthenol.

    FOR ANIMAL USE ONLY

    KEEP OUT OF REACH OF CHILDREN

    TAKE TIME OBSERVE LABEL DIRECTIONS

  • DOSAGE & ADMINISTRATION

    DOSAGE AND ADMINISTRATION:
    Dogs and Cats: 25 mg per 5 lbs. body weight intramuscularly.
    Horses: Initial dose 10 cc intravenously or intramuscularly.

  • PRECAUTIONS

    PRECAUTION: Following the administration of succinylcholine chloride, a one-hour waiting period is advisable before initiation of dexpanthenol therapy.

  • CONTRAINDICATIONS

    CONTRAINDICATIONS: In therapy of colic resulting from the administration of cholinergic type anthelmintics.

  • PRINCIPAL DISPLAY PANEL

    Dexpanthenol Injection 100 mL

  • INGREDIENTS AND APPEARANCE
    DEXPANTHENOL 
    dexpanthenol injection, solution
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:54925-064
    Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXPANTHENOL (UNII: 1O6C93RI7Z) (DEXPANTHENOL - UNII:1O6C93RI7Z) DEXPANTHENOL250 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54925-064-10100 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/01/2008
    Labeler - Med-Pharmex, Inc (025353699)