Label: GUAIFENESIN STRAWBERRY-BANANA FLAVOR- guaifenesin liquid

  • NDC Code(s): 71800-059-19
  • Packager: Innovida Pharmaeutique Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 18, 2025

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  • Active Ingredient 

    Guaifenesin,USP 100 mg (in each 5ml tsp)

  • Purpose

    Expectorant

  • Uses

    • helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive
  • Warnings

    Do not take this product for persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema, or where cough is accompanied by excessive phlegm (mucus) unless directed by a doctor.

    Stop use and ask a doctor if■ cough persists for more than a week, tends to recur, or is accompanied by a fever, rash or persistent headache, consult a doctor. A persistent cough may be a sign of a serious condition.

    If pregnant or breast-feeding, ask a health professional before use. Keep out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • KEEP OUT OF REACH OF CHILDREN

  • Directions

    • Do not take more than 6 doses in any 24 hours period
     age dose

     Adults and Children 12 years of age and over:

    Children under 12 years of age:

     Take 2-4 teaspoonful (5mL) every 4 hours

    Consult a physician

  • Other Information

    • store at room temperature ■ 15°-30°C (59°-86°F)
    • TAMPER-EVIDENT: Do not use if seal under cap is torn, broken or missing.
  • Inactive Ingredients

    Citric acid, FD&C yellow #5, glycerin, methylparaben, potassium sorbate, propylene glycol, propylparaben, purified water, sodium citrate, strawberry-banana flavor, sucralose.

  • Questions or Comments? 1-888-462-4166

  • Product label

    image description

  • INGREDIENTS AND APPEARANCE
    GUAIFENESIN STRAWBERRY-BANANA FLAVOR 
    guaifenesin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71800-059
    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
    CITRIC ACID (UNII: 2968PHW8QP)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MENTHOL (UNII: L7T10EIP3A)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    STRAWBERRY (UNII: 4J2TY8Y81V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71800-059-19119 mL in 1 TUBE; Type 0: Not a Combination Product06/16/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01206/16/2025
    Labeler - Innovida Pharmaeutique Corporation (080892908)
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