Label: MENTHOL DROPS DOLLAR GENERAL SEVERE 45CT- menthol lozenge

  • NDC Code(s): 75712-040-01
  • Packager: Dollar General Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 12, 2024

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

  • Drug Facts

  • Active ingredient 

    Menthol 20 mg

    Purpose

    Oral anesthetic

  • Uses

    Temporarily relieves occasional minor irritation and pain due to: sore throat; sore mouth

  • Warnings

    Sore throat warning: ore throat warning: severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea and vomiting may be serious. Consult doctor promptly. Do not use more than 2 days or administer to children under 12 years of age.

    Ask a doctor before use if you have:

    • a severe sore throat accompanied by difficult in breathing or that lasts more than 2 days 
    • a sore accompanied by fever, headache, rash, swelling, nausea or vomiting

    Stop use and ask a doctor if

    • sore mouth symptoms do not improve in 7 days, or if irritation, pain or redness lasts or worsens

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

    Keep out of reach of children.

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

  • Directions

     adults and children 12 years and over  dissolve 1 lozenge slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor.
     children under 12 years  do not use

  • 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
    MENTHOL DROPS DOLLAR GENERAL SEVERE 45CT 
    menthol lozenge
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75712-040
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL20 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:75712-040-019 in 1 CARTON03/15/2024
    145 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)