Label: MUCOSAN MULTI-SYMPTOM CHERRY- dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride liquid

  • NDC Code(s): 53145-693-04
  • Packager: Menper Distributors, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 12, 2024

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  • INACTIVE INGREDIENT

    Active ingredients (in each 5 mL or teaspoon) Purpose

    Dextromethorphan HBr, 10 mg..............................Cough suppressant

    Guaifenesin, 100 mg..............................................Expectorant

    Phenylephrine HCl, 5 mg.......................................Nasal decongestant

  • PURPOSE

    Purposes

    Cough suppressant

    Expectorant

    Nasal decongestant

  • INDICATIONS & USAGE

    Uses

    • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
    • temporarily relieves these symptoms occuring with a cold:
    • nasal congestion
    • cough due to minor throat and bronchial irritation
  • WARNINGS

    Warnings

    Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

  • ASK DOCTOR

    Ask a doctor before use if you have

    • heart disease
    • high blood pressure
    • thyroid disease
    • diabetes
    • trouble urinating due to an enlarged prostate gland
    • cough that occurs with too much phlegm (mucus)
    • cough that lasts or is chronic such as occurs with smoking, asthma, chornic bronchitis or emphysema
  • ASK DOCTOR/PHARMACIST

    Ask a doctor or pharmacist before use if you are

    taking any other oral nasal decongestant or stimulant.

  • OVERDOSAGE

    Do not exceed recommended dosage.

  • STOP USE

    Stop use and ask a doctor if

    • you get nervous, dizzy or sleepless
    • symptoms do not get better within 7 days or are accompanied by fever
    • cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistant headache. These could be signs of a serious condition.
  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast - feeding, ask a helath 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.

  • DOSAGE & ADMINISTRATION

    Directions

    • do not take more than 6 doses in any 24 hour period
    • this adult stregth product is not intended for use in children under 12 years of age
    • measure only with dosing cup provided
    • keep dosing cup with product
    • TSP=teaspoon

    agedose
    adults and children 12 years and over2 teaspoons (10mL) every 4 hours
    children under 12 yearsdo not use

  • OTHER SAFETY INFORMATION

    Ohter information

    • each teaspoon (5mL) contains: sodium 3 mg
    • store at 15-30°C (59-86°F). Do not refrigetate.
  • INACTIVE INGREDIENT

    anhydrous citric acid, FD&C red #40, flavor, glycerin, menthol, propylene glycol, purified water, sodium benzoate, sorbitol solution, sucralose

  • QUESTIONS

    Questions or comments?

    1-800-560-5223 Monday to Friday 9am-4pm, Eastern Time

  • PRINCIPAL DISPLAY PANEL

    MUCOSAN MULTI SYMPTOM LABELMUCOSAN MULTI SYMPTOM BOX

  • INGREDIENTS AND APPEARANCE
    MUCOSAN MULTI-SYMPTOM CHERRY 
    dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53145-693
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 5 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg  in 5 mL
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    MENTHOL (UNII: L7T10EIP3A)  
    SORBITOL SOLUTION (UNII: 8KW3E207O2)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53145-693-041 in 1 CARTON11/01/2024
    1118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01211/01/2024
    Labeler - Menper Distributors, Inc. (101947166)
    Registrant - Menper Distributors, Inc. (101947166)
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