Label: NO HAPPY DREAM (HELPS IMPROVE SLEEP, LETTUCE AND CHAMOMILE FERMENTED POWDER)- nitric oxide, vitamin d3, glutathione capsule

  • 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

    420 mg X 90
    / 1.33 oz

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF THE REACH OF CHILDREN.

  • INDICATIONS & USAGE

    N:O Happy Dream

  • WARNINGS

    Warnings

  • PURPOSE

    N:O Happy Dream

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Rice bran extract powder, yeast extract, Microcrystalline cellulose

  • ACTIVE INGREDIENT

    Active ingredients:

    Nitric Oxide, Vitamin D3, Glutathione

  • PRINCIPAL DISPLAY PANEL

    5

  • INGREDIENTS AND APPEARANCE
    NO HAPPY DREAM (HELPS IMPROVE SLEEP, LETTUCE AND CHAMOMILE FERMENTED POWDER) 
    nitric oxide, vitamin d3, glutathione capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83202-6255
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NITRIC OXIDE (UNII: 31C4KY9ESH) (NITRIC OXIDE - UNII:31C4KY9ESH) NITRIC OXIDE100 mg  in 420 mg
    Inactive Ingredients
    Ingredient NameStrength
    YEAST (UNII: 3NY3SM6B8U) 1 mg  in 420 mg
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) 1 mg  in 420 mg
    Product Characteristics
    ColorwhiteScorescore with uneven pieces
    ShapeCAPSULESize420mm
    FlavorFRUITImprint Code capsule
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83202-6255-190 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(83202-6255)