Label: TUSSIN COUGH EXPECTORANT COUGH SUPRESSANT DM- dextromethorphan hydrobromide, guaifenesin liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 29, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • Drug FactsActive ingredients ( in each 5 mL tsp)

    Dextromethorphan HBr, USP 10 mg

    Guaifenesin, USP 100 mg

  • Purpose

    Cough Suppressant
    Expectorant

  • 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

  • Uses

    • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
    • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
  • Warnings

    Do not use

    • in a child under 12 years of age
    • 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 A Doctor Before You Use if You Have

    • cough that occurs with too much phlegm (mucus)
    • cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema
  • Stop Use And Ask A Doctor If

    cough lasts more than 7 days, comes back or is accompanied by fever, rash or persistent headache. These could be signs of a serious condition.

  • If Pregnant Or Breast-Feeding

    ask a health professional before use.

  • Directions

    •  do not take more than 6 doses in any 24-hour period

    Age                                       Dose

    adults & children                     2 teaspoonfuls
    12 years and over                  every 4 hours

    children under 12 years           do not use

  • Other information

    • store at 20-25° C (66-77° F)
    • do not refrigerate
    • dosage cup provided
    • sodium 3 mg per teaspoon
  • Inactive ingredients

    Anhydrous citric acid, dextrose, FD & C red # 40, flavor, glycerin, high fructose corn syrup, menthol, purified water, saccharin sodium, sodium benzoate

  • Questions?

    Call weekdays from 9:30 AM to 4:30 PM EST at

    1-877-798-5944

  • Tussin Cough DM product label

    * COMPARE TO ROBITUSSIN® PEAK COLD ACTIVE INGREDIENTS


    CVP® CONSUMER VALUE PRODUCTS

    TUSSIN COUGH EXPECTORANT COUGH SUPPRESSANT DM

    NON-DROWSY COUGH FORMULA

    • ADULT
    • FOR AGES 12 AND OVER
    • CONTROLS COUGH
    • HELPS LOOSEN CHEST CONGESTION

    4 FL OZ (118 Ml)

    * This product is not manufactured or distributed by Pfizer, owner of the registered trademark Robitussin® Peak Cold

    Box-001 Rev 01

    DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING

    Distributed by: Salado Sales, Inc.  P.O. Box 6115 Temple, TX 76503  www.saladosales.com

    LOT.

    EXP.

    AptaSS TussinDM 503

    AptaSS TussinDM 503 1

    res

    AptaSS TussinDM 503

    AptaSS TussinDM 503 1

  • INGREDIENTS AND APPEARANCE
    TUSSIN COUGH  EXPECTORANT COUGH SUPRESSANT DM
    dextromethorphan hydrobromide, guaifenesin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57243-503
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 5 mL
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    MENTHOL (UNII: L7T10EIP3A)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57243-503-24118 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01201/01/2012
    Labeler - Salado Sales, Inc. (009830555)
    Registrant - AptaPharma Inc. (790523323)
    Establishment
    NameAddressID/FEIBusiness Operations
    AptaPharma Inc.790523323manufacture(57243-503)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!