Label: NATURAL CHERRY HONEY HERB THROAT DROPS- menthol lozenge

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

Drug Label Information

Updated December 5, 2024

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  • Drug Facts

    Purpose

    Oral pain reliever

  • Active Ingredient (in each drop)

    Menthol, 1.8 mg

  • Uses

    temporarily relieves occasional minor irritation and pain associated with:

    • sore mouth
    • sore throat
  • Warnings

    Do not use

    • in children under 6 years of age unless directed by a doctor.
  • Stop use and ask a doctor if

    • sore throat is severe, persists for more than 2 days, or is accompanied by fever, headache, rash, nausea or vomiting
    • sore mouth symptoms do not improve in 7 days
  • Keep out of reach of children.


  • Directions

    • adults and children 6 years and older:  dissolve 2 drops (one at a time) slowly in the mouth.  Repeat every 2 hours as needed or as directed by a doctor
    • children under 6 years: ask a doctor
  • Inactive Ingredients

    extract of a Ricola herb mixture (elder, horehound, hyssop, lemon balm, linden flowers, mallow, peppermint, sage, thyme, wild thyme), honey, malic acid, natural cherry concentrate, natural color (extract of fruit and vegetable), natural flavors, starch syrup, sugar
  • PRINCIPAL DISPLAY PANEL

    Image of STG_ETGD_KIRHO_37G_US_9008621_Final.jpg

  • INGREDIENTS AND APPEARANCE
    NATURAL CHERRY HONEY HERB THROAT DROPS 
    menthol lozenge
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54305-507
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1.8 mg
    Inactive Ingredients
    Ingredient NameStrength
    MALIC ACID (UNII: 817L1N4CKP)  
    HONEY (UNII: Y9H1V576FH)  
    CHERRY (UNII: BUC5I9595W)  
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorredScoreno score
    ShapeOVALSize24mm
    FlavorCHERRY (CHERRY, ALMOND, HONEY) Imprint Code R
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54305-507-1010 in 1 PACKAGE; Type 0: Not a Combination Product01/01/1942
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02201/01/1942
    Labeler - Ricola Ag (480227248)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ricola Ag485393768manufacture(54305-507)
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