Label: DRY MOUTH MOISTURIZINGSPRAY liquid

  • NDC Code(s): 84025-267-01
  • Packager: Guangzhou Yanxi Biotechnology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 22, 2024

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  • DOSAGE & ADMINISTRATION

    Spray directly into mouth on the tongue.Rub tongue over teeth and gums for at least 5 seconds.Use as needed.

  • WARNINGS

    Keep out of children

  • INACTIVE INGREDIENT

    Aqua

  • INDICATIONS & USAGE

    For daily oral care

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of children

  • PURPOSE

    Rapidlyl, moistens and soothes

  • PRINCIPAL DISPLAY PANEL

    84025-267

  • INGREDIENTS AND APPEARANCE
    DRY MOUTH MOISTURIZINGSPRAY 
    dry mouth moisturizingspray liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84025-267
    Route of AdministrationCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2 mg  in 50 mL
    XYLITOL (UNII: VCQ006KQ1E) (XYLITOL - UNII:VCQ006KQ1E) XYLITOL3 mg  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84025-267-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product11/22/2024
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02211/22/2024
    Labeler - Guangzhou Yanxi Biotechnology Co., Ltd (632583102)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Yanxi Biotechnology Co., Ltd632583102manufacture(84025-267)
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