Label: AKIN EXPECTORANT FORMULA STRAWBERRY BANANA- guaifenesin liquid

  • NDC Code(s): 69822-212-04
  • Packager: Southern Sales & Service, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 29, 2023

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  • Drug Facts

  • Active ingredient (in each 5ml tsp.)

    Guaifenesin USP 100 mg

    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 direct 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 persistant headache, consult a doctor. A persistent cough may be a sign of a serious condition.

    If pregnant or beast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions

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

    Adults and children 12 years and overTake 2-4 teaspoonful (5mL) every 4 hours
    Children under 12 yearsConsult a physician
  • Other information

    • store at room temperature • 15°-30°C (59°-86°F)

    Do not use if seal under cap is torn, broken or missing. TAMPER-EVIDENT:

  • Inactive ingredients

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

  • Package Labeling:

    Label2

  • INGREDIENTS AND APPEARANCE
    AKIN EXPECTORANT FORMULA STRAWBERRY BANANA 
    guaifenesin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69822-212
    Route of AdministrationTOPICAL
    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 MONOHYDRATE (UNII: 2968PHW8QP)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69822-212-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product02/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01202/01/2023
    Labeler - Southern Sales & Service, Inc. (013114906)
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