Label: COUGH DROPS DOLLAR GENERAL MENTHOL 80CT- menthol lozenge

  • NDC Code(s): 75712-034-01
  • Packager: Dollar General Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 12, 2024

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  • Drug Facts

  • Active ingredient (in each drop)

    Menthol 5.4 mg

    Purpose

    Cough suppressant/Oral anesthetic

  • Uses

    • temporarily relieves:
    • cough as may occur with a cold
    • occasional minor irritation and sore throat
  • Warnings

    Sore throat warning:if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. If sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. These symptoms may be serious.

    Ask a doctor before use if you have:

    • persistent or chronic cough such as occurs with smoking, asthma, or emphysema
    • cough accompanied by excessive phlegm (mucus)

    Stop use and ask a doctor if

    • cough persists for more than 7 days, tends to recur, or is accompanied by fever, rash, or persistent headache, These could be signs of a serious condition.
    • sore throat is severe, or irritation, pain or redness lasts or worsens
    • sore mouth does not improve in 7 days

    If pregnant or breast-feeding
    ask a health professional before use.

    Keep out of reach of children.

  • Directions

     adults and children 5 years and over  dissolve 1 lozenge slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor.
     children under 5 years  ask a doctor 

  • Other information

    • 11 calories per drop
    • do not use if bags is torn or open
    • Contains: Soy
  • Inactive ingredients

    Corn Syrup, eucalytus oil, FD&C blue no. 1, FD&C red no. 40, Gum Arabic, Maltodextrin, natural flavor, soy lecithin,  sucrose and water

  • Product label

    image description

  • INGREDIENTS AND APPEARANCE
    COUGH DROPS DOLLAR GENERAL MENTHOL 80CT 
    menthol lozenge
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75712-034
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL5.4 mg
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    CORN SYRUP (UNII: 9G5L16BK6N)  
    EUCALYPTOL (UNII: RV6J6604TK)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    ACACIA (UNII: 5C5403N26O)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    Product Characteristics
    ColorblueScoreno score
    ShapeOVALSize20mm
    FlavorMENTHOLImprint Code F
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75712-034-016 in 1 CARTON03/15/2024
    180 in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01203/15/2024
    Labeler - Dollar General Corporation (006946172)
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