Label: FATHER JOHNS COUGH MEDICINE PLUS- nasal decongestant liquid

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 18, 2023

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  • ACTIVE INGREDIENT

    Each 30 mL (2 tablespoonfuls) contain:

    Dextromethorphan HBr, 10mg

    Phenylephrine HCl, 10mg

    Chlorpheniramine Maleate, 4mg

  • INACTIVE INGREDIENT

    Citric acid

    FD&C Red #40

    FD&C Blue #1

    Glycerin

    Purified water

    Sodium benzoate

    Sodium chloride

    Sodium citrate

    Sodium saccharin

    Sucrose

  • DOSAGE & ADMINISTRATION

    DO NOT take more than 12 tablespoonfuls in 24 hours

    Adults and Children 12 years and older: take 2 tablespoons every 4 hours

    Children under 12 years old: ask a doctor

  • INDICATIONS & USAGE

    For temporarily relief of couch and allergy symptoms, including coughing, nasal congestion, and runny nose.

  • WARNINGS

    WARNINGS: Do not excees recommended dosage

  • PURPOSE

    Cough Supressant

    Nasal Decongestant

    Anthihistamine

  • 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.

  • PRINCIPAL DISPLAY PANEL

    Father Johns Plus 4oz 2022fatherplus '

  • INGREDIENTS AND APPEARANCE
    FATHER JOHNS COUGH MEDICINE PLUS 
    nasal decongestant liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:45728-445
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 30 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg  in 30 mL
    CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE4 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SUCROSE (UNII: C151H8M554)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:45728-445-941 in 1 CARTON06/17/2019
    1118 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01206/17/2019
    Labeler - Oakhurst Company (001385111)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114label(45728-445) , pack(45728-445) , analysis(45728-445) , manufacture(45728-445)
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