Label: ismotic- isosorbide solution

  • Category: HUMAN PRESCRIPTION DRUG LABEL

Drug Label Information

Updated March 23, 2006

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  • N/A - Section Title Not Found In Database

  • DESCRIPTION

    ISMOTIC® is a 45% w/v solution of isosorbide in a vanilla-mint flavored vehicle. ISMOTIC is a caramel colored aqueous solution that is chemically stable at room temperature.

    Each mL contains:

    Isosorbide 45% w/v (Isosorbide Concentrate 60.6%), Alcohol 0.3% w/v, Caramel, Creme de Menthe, Malic Acid, Potassium Citrate, Potassium Sorbate, Saccharin Calcium, Sodium Citrate, Sorbitol Solution, Vanilla Concentrate Imitation #20, Potassium Hydroxide (to adjust pH), and Purified Water.

    DM-00

    Typical analysis of electrolyte content:

    4.6 meq. of Sodium/220 mL ISMOTIC Solution

    0.9 meq. of Potassium/220 mL ISMOTIC Solution

    Isosorbide, the osmotic agent in ISMOTIC, is a dihydric alcohol with the formula C6H10O4 represented by the structure:

    Image from Drug Label Content

  • CLINICAL PHARMACOLOGY

    Isosorbide is rapidly absorbed after oral administration. It is essentially nonmetabolized, and in the circulation, it contributes to the tonicity of the blood until it is eliminated by the kidney unchanged. While in the blood, isosorbide acts as an osmotic agent to promote redistribution of water toward the circulation with ultimate elimination in the urine. The physical action of ISMOTIC is similar to that of other osmotic drugs.

  • INDICATIONS AND USAGE

    For the short-term reduction of intraocular pressure. May be used prior to and after intraocular surgery. May be used to interrupt an acute attack of glaucoma.

  • CONTRAINDICATIONS

    1. Well-established anuria
    2. Severe dehydration
    3. Frank or impending acute pulmonary edema
    4. Severe cardiac decompensation
    5. Hypersensitivity to any component of this preparation
  • WARNINGS

    1. With repeated doses, consideration should be given to maintenance of adequate fluid and electrolyte balance.
    2. If urinary output continues to decrease, the patient’s clinical status should be closely reviewed. Accumulation of ISMOTIC may result in overexpansion of the extracellular fluid.
  • PRECAUTIONS

    General

    For oral use only – not for injection. Repetitive doses should be used with caution particularly in patients with diseases associated with salt retention. Ensure that patient’s bladder has been emptied prior to surgery.

    Carcinogenesis, Mutagenesis, Impairment of Fertility

    No studies have been conducted in animals or in humans to evaluate the potential of these effects.

    Pregnancy

    Pregnancy Category B

    Reproduction (fertility and teratology) studies have been performed in rats at doses approximately 5 times the recommended initial human dose of 1.5 gm/kg body weight and have revealed no evidence of impaired fertility or harm to the fetus due to isosorbide. Teratology studies have been performed with rabbits and rats given daily oral doses of isosorbide at 6.5 and 10 times, respectively, the recommended initial human dose during organogenesis without evidence of harm to the fetus. There are, however, no adequate and well-controlled studies in pregnant women. Because animal studies are not always predictive of human responses, this drug should be used during pregnancy only if clearly needed.

    Nursing Mothers

    It is not known whether this drug is excreted in human milk. Because many drugs are excreted in breast milk, caution should be exercised when isosorbide is administered to a nursing mother.

    Pediatric Use

    Safety and effectiveness in pediatric patients have not been established.

  • ADVERSE REACTIONS

    Nausea, vomiting, headache, confusion, and disorientation may occur. Occurrences of syncope, gastric discomfort, lethargy, vertigo, thirst, dizziness, hiccups, hypernatremia, hyperosmolarity, irritability, rash and light-headedness have been reported.

  • DOSAGE AND ADMINISTRATION

    The recommended initial dose of isosorbide is 1.5 gm/kg body weight (equivalent to 1.5 mL /lb. of body weight). The onset of action is usually within 30 minutes while the maximum effect is expected at 1 to 1 1/2 hours. The useful dose range is 1 to 3 gm/kg body weight and the drug effect will persist up to 5 to 6 hours. Use two to four times a day as indicated. Palatability may be improved if the medication is poured over cracked ice and sipped.

    RECOMMENDED DOSAGES ARE:

    POUNDSMILLILITERSPOUNDSMILLILITERS
    100150155235
    105155160240
    110165165250
    115170170255
    120180175265
    125190180270
    130195185280
    135205190285
    140210195295
    145220200300
    150225
  • HOW SUPPLIED

    Disposable plastic bottles of 220 mL (100 gm of isosorbide/220 mL) for oral use only.

    NDC 0065-0034-08

    Storage: Store at 15°-30°C (59°-86°F).

    CAUTION: Federal ( USA) law prohibits dispensing without prescription.

    Mfd. for: Alcon Laboratories, Inc.

    Fort Worth, Texas 76134 USA

    Mfd. by: ALCON (Puerto Rico) INC.

    Humacao, Puerto Rico 00791 USA

    July 1997      Printed in USA

    249165-0797

  • INGREDIENTS AND APPEARANCE
    ISMOTIC 
    isosorbide solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0065-0034
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    isosorbide (UNII: WXR179L51S) (isosorbide - UNII:WXR179L51S) 450 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    alcohol (UNII: 3K9958V90M)  
    caramel (UNII: T9D99G2B1R)  
    crème de menthe ()  
    malic acid (UNII: J3TZF807X5)  
    potassium citrate (UNII: EE90ONI6FF)  
    potassium sorbate (UNII: 1VPU26JZZ4)  
    saccharin calcium (UNII: 5101OP7P2I)  
    sodium citrate (UNII: 1Q73Q2JULR)  
    sorbitol solution ()  
    vanilla concentrate imitation #20 ()  
    potassium hydroxide (UNII: WZH3C48M4T)  
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0065-0034-08220 mL in 1 BOTTLE, PLASTIC
    Labeler - Alcon Laboratories, Inc.