Label: PROBIOTIC BRIGHTENING paste

  • NDC Code(s): 84732-020-01
  • Packager: Dongguan Haiyi Technology Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 27, 2024

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

  • Active ingredient

    Lactobacillus Ferment

  • Inactive ingredient

    Glycerin ,Sodium Lauryl Sulfate

  • Purpose section

    Go To Halitosis;

    BRIGHT WHITE TEETH;

    REMOVE BAD BREATH;

  • Warning

    Keep out of reach of children.
    Avoid direct contact with eyes.
    Discontinue use if irritationoccurs

    Store in a cool and dry place.

  • stop use

    This product may cause allergic reactions in asmall number of people.
    lf youexperience any discomfort,please stop using it immediately.

  • not use

    Not suitable for use by children, pregnantor breastfeeding people.

  • OUT OF CHILDREN

    KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

  • HOW TO USE

    Take an appropriate amount oftoothpaste on the toothbrush.Gently brush your teeth in circularmotions frominside to outside for 1-2 minutes.Rinse with clean water.

  • Dosage

    Give it twice a day, once in the morning and evening

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    PROBIOTIC BRIGHTENING 
    probiotic brightening paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84732-020
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP) (LIMOSILACTOBACILLUS FERMENTUM - UNII:2C1F12C6AP) LIMOSILACTOBACILLUS FERMENTUM1 g  in 120 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84732-020-01120 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/27/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02209/27/2024
    Labeler - Dongguan Haiyi Technology Co.,Ltd. (722030807)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dongguan Haiyi Technology Co.,Ltd.722030807manufacture(84732-020)