Label: LIQUID liquid

  • NDC Code(s): 84067-514-01
  • Packager: Shantou Youjia E-Commerce Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated March 15, 2024

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  • PRINCIPAL DISPLAY PANEL

    Package label

  • INGREDIENTS AND APPEARANCE
    LIQUID 
    liquid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84067-514
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LACTICASEIBACILLUS PARACASEI CNCM I-4034 (UNII: Z53BZW9PCN) (LACTICASEIBACILLUS PARACASEI CNCM I-4034 - UNII:Z53BZW9PCN) LACTICASEIBACILLUS PARACASEI CNCM I-40340.35 mg  in 4 mg
    GREEN TEA LEAF (UNII: W2ZU1RY8B0) (GREEN TEA LEAF - UNII:W2ZU1RY8B0) GREEN TEA LEAF0.7 mg  in 4 mg
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2.1 mg  in 4 mg
    PROPOLIS WAX (UNII: 6Y8XYV2NOF) (PROPOLIS WAX - UNII:6Y8XYV2NOF) PROPOLIS WAX1.05 mg  in 4 mg
    PYRITHIOBAC-SODIUM (UNII: 5M13LUJ9WY) (PYRITHIOBAC-SODIUM - UNII:5M13LUJ9WY) PYRITHIOBAC-SODIUM1.4 mg  in 4 mg
    MINT (UNII: FV98Z8GITP) (MINT - UNII:FV98Z8GITP) MINT1.05 mg  in 4 mg
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 0.35 mL  in 4 mg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84067-514-014 mg in 1 BOX; Type 0: Not a Combination Product02/01/202412/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Export only02/01/202412/31/2024
    Labeler - Shantou Youjia E-Commerce Co.,Ltd. (711173127)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shantou Youjia E-Commerce Co.,Ltd.711173127label(84067-514)