Label: BRONCOMAR EXPECTORANT SF- guaifenesin liquid

  • NDC Code(s): 70242-100-06
  • Packager: Dannso Corp./d.b.a. Essential Products
  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated January 1, 2016

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  • ACTIVE INGREDIENT

    Active Ingredients:(in each 5 ml.)Purpose

    Guaifenesin 100 mg.......................................................

    Expectorant

  • PURPOSE

    Uses:

    • Helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make cough more productive.
  • WARNINGS

    Warnings

    Do not exceed recommended dosage

  • ASK DOCTOR

    Ask doctor before use if you have

    • Cough that occurs with too much phlegm(mucus)
    • Cough that last or is a chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema.
  • Ask a doctor before use

    • Nervousness, dizziness or sleeplessness occurs.
    • Cough persists more than 1 week, tends to recur or is accompanied by a fever, rash or persistent headache. A persistent cough may be sign serious condition.
  • Do not use

    • If you have a chronic pulmonary disease or shortness of breath unless directed by a doctor.
  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding ask a health professional before use.


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away. Avoid alcoholic beverages while using this product.

  • DOSAGE & ADMINISTRATION

    Directions

    • Do not exceed 6 doses in any 24 hour period.
    • Shake well before use

    AGE
    DOSE
    Adults and Children 12 years and over
    10 ml (2 tsps) every 4 hours
    Children 6 to under 12 years of age
    5 ml (1 tsp) every 4 hours
    Children under 6 years of age
    Do not  use
  • INDICATIONS & USAGE

    Other Information:

    • Each 5 mls contains: sodium 8 mg
    • Store between 15 - 30 degrees Celsius (59 - 86 Fahrenheit).
    • Tamper Evident Feature:Do not use if seal under cap is torn, broken or missing.
  • Inactive Ingredient

    Blue Cohosh, Citric Acid, Echinacea Oil, Ginkgo Biloba, Glycerin Seal Root, Honey Flavor, Horehound Herb, Licorice, Golden Seal Root, Menthol, Mullein, Myrrh, Potassium Sobate, Slippery Elm Bark, Sodium Benzoate, Propylene Glycol, Purifed Water, sodium Chloride, Sucralose, Wild Cheery bark, and Zinc Sulfate.

  • Questions or Comments

    Call Weekdays from 9:30 AM to 5PM EST at Tel 305-261-762

    Distributed by

    Essential Products Miami FL 33126

    www.jjjdistributors.com

    Made in U.S.A.

  • PRINCIPAL DISPLAY PANEL

    Broncomar Expectorant SF

  • INGREDIENTS AND APPEARANCE
    BRONCOMAR EXPECTORANT  SF
    guaifenesin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70242-100
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ECHINACEA (UNII: 4N9P6CC1DX)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    GINKGO (UNII: 19FUJ2C58T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GOLDENSEAL (UNII: ZW3Z11D0JV)  
    HONEY (UNII: Y9H1V576FH)  
    HOREHOUND (UNII: K08036XEJV)  
    LICORICE (UNII: 61ZBX54883)  
    MENTHOL (UNII: L7T10EIP3A)  
    VERBASCUM THAPSUS (UNII: C9TD27U172)  
    MYRRH (UNII: JC71GJ1F3L)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    ULMUS RUBRA BARK (UNII: 91QY4PXU8Q)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    PRUNUS SEROTINA BARK (UNII: 5D48E975HA)  
    ZINC SULFATE (UNII: 89DS0H96TB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70242-100-061 in 1 CARTON01/01/2015
    1177 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34110/01/2001
    Labeler - Dannso Corp./d.b.a. Essential Products (059741071)
    Registrant - Dannso Corp./d.b.a. Essential Products (059741071)
    Establishment
    NameAddressID/FEIBusiness Operations
    All Pharma LLC078572520MANUFACTURE(70242-100)