Label: DR. NO I (WOUND RECOVERY, BURN WOUND RECOVERY, ACNE TREATMENT, FERMENTED LETTUCE EXTRACT CONCENTRATE)- nitric oxide liquid

  • 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

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  • DOSAGE & ADMINISTRATION

  • ACTIVE INGREDIENT

  • INDICATIONS & USAGE

  • WARNINGS

  • PURPOSE

  • INACTIVE INGREDIENT

  • ACTIVE INGREDIENT

  • KEEP OUT OF REACH OF CHILDREN

  • PRINCIPAL DISPLAY PANEL

    34

  • INGREDIENTS AND APPEARANCE
    DR. NO I (WOUND RECOVERY, BURN WOUND RECOVERY, ACNE TREATMENT, FERMENTED LETTUCE EXTRACT CONCENTRATE) 
    nitric oxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83202-6841
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NITRIC OXIDE (UNII: 31C4KY9ESH) (NITRIC OXIDE - UNII:31C4KY9ESH) NITRIC OXIDE20 mg  in 30 mg
    Inactive Ingredients
    Ingredient NameStrength
    LETTUCE (UNII: 5PO6NN3RRJ) 1 mg  in 30 mg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83202-6841-330 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(83202-6841)