Label: BIO NO MORE YEAST INFECTION (HELPS IMPROVE VAGINAL YEAST INFECTION, FERMENTED CABBAGE POWDER)- nitric oxide, vitamin d3, glutathione tablet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated March 19, 2024

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

  • DOSAGE & ADMINISTRATION

    900 mg / 0.032oz

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF THE REACH OF CHILDREN.

  • INDICATIONS & USAGE

    Bio NO more Yeast infection (Helps improve vaginal yeast infection, fermented Cabbage powder)

  • WARNINGS

    Warnings

  • PURPOSE

    Bio NO more Yeast infection (Helps improve vaginal yeast infection, fermented Cabbage powder)

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Glutathione, lettuce, Garlic

  • ACTIVE INGREDIENT

    Active ingredients:

    Nitric Oxide, Vitamin D3, Glutathione

  • PRINCIPAL DISPLAY PANEL

    37

  • INGREDIENTS AND APPEARANCE
    BIO NO MORE YEAST INFECTION (HELPS IMPROVE VAGINAL YEAST INFECTION, FERMENTED CABBAGE POWDER) 
    nitric oxide, vitamin d3, glutathione tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83202-6447
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NITRIC OXIDE (UNII: 31C4KY9ESH) (NITRIC OXIDE - UNII:31C4KY9ESH) NITRIC OXIDE100 mg  in 900 mg
    Inactive Ingredients
    Ingredient NameStrength
    LETTUCE (UNII: 5PO6NN3RRJ) 1 mg  in 900 mg
    GLUTATHIONE (UNII: GAN16C9B8O) 1 mg  in 900 mg
    GARLIC (UNII: V1V998DC17) 1 mg  in 900 mg
    Product Characteristics
    ColorwhiteScorescore with uneven pieces
    ShapeCAPSULESize900mm
    FlavorFRUITImprint Code capsule
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83202-6447-2900 mg in 1 PACKAGE; Type 0: Not a Combination Product03/20/202403/19/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/20/202403/19/2025
    Labeler - HumanEnos LLC (695801540)
    Establishment
    NameAddressID/FEIBusiness Operations
    HumanEnos LLC695801540manufacture(83202-6447)