Label: HEXALONG NO (HELPS HEMATOPOIESIS AND IMMUNITY, HEXALONG FERMENTED POWDER)- nitric oxide, zinc, vitamin d3 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 February 12, 2024

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

  • DOSAGE & ADMINISTRATION

    500 mg X 120
    / 2.12 oz

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF THE REACH OF CHILDREN.

  • INDICATIONS & USAGE

    Hexalong N:O

  • WARNINGS

    Warnings

  • PURPOSE

    Hexalong N:O

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Corn Starch, Dietary fiber, beet red concentratd powder

  • ACTIVE INGREDIENT

    Active ingredients:

    Nitric Oxide, Zinc, Vitamin D3

  • PRINCIPAL DISPLAY PANEL

    6

  • INGREDIENTS AND APPEARANCE
    HEXALONG NO (HELPS HEMATOPOIESIS AND IMMUNITY, HEXALONG FERMENTED POWDER) 
    nitric oxide, zinc, vitamin d3 tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83202-5578
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NITRIC OXIDE (UNII: 31C4KY9ESH) (NITRIC OXIDE - UNII:31C4KY9ESH) NITRIC OXIDE100 mg  in 500 mg
    Inactive Ingredients
    Ingredient NameStrength
    BEET (UNII: N487KM8COK) 1 mg  in 500 mg
    MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T) 1 mg  in 500 mg
    Product Characteristics
    ColorwhiteScorescore with uneven pieces
    ShapeCAPSULESize500mm
    FlavorFRUITImprint Code tablet
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83202-5578-2120 mg in 1 PACKAGE; Type 0: Not a Combination Product02/13/202402/12/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/13/202402/12/2025
    Labeler - HumanEnos LLC (695801540)
    Establishment
    NameAddressID/FEIBusiness Operations
    HumanEnos LLC695801540manufacture(83202-5578)