Label: NO MORE DRIP FOR NOSE COMFORT (RELIEVES NASAL CONGESTION, SINUS CONGESTION, REHYDRATE NASAL PASSAGES, ALLERGY RELIEF, CONCENTRATED LETTUCE FERMENTATION)- ntric 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

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

  • DOSAGE & ADMINISTRATION

    20 ml/ 0.7 oz

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF THE REACH OF CHILDREN

  • INDICATIONS & USAGE

    N:O more Drip Nasal Spray

  • WARNINGS

    Warnings

  • PURPOSE

    N:O more Drip Nasal Spray

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Lettuce

  • ACTIVE INGREDIENT

    Active ingredients:

    Ntric Oxide

  • PRINCIPAL DISPLAY PANEL

    7

  • INGREDIENTS AND APPEARANCE
    NO MORE DRIP FOR NOSE COMFORT (RELIEVES NASAL CONGESTION, SINUS CONGESTION, REHYDRATE NASAL PASSAGES, ALLERGY RELIEF, CONCENTRATED LETTUCE FERMENTATION) 
    ntric oxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83202-1469
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NITRIC OXIDE (UNII: 31C4KY9ESH) (NITRIC OXIDE - UNII:31C4KY9ESH) NITRIC OXIDE10 mg  in 20 mg
    Inactive Ingredients
    Ingredient NameStrength
    LETTUCE (UNII: 5PO6NN3RRJ) 1 mg  in 20 mg
    Product Characteristics
    ColorwhiteScorescore with uneven pieces
    ShapeCAPSULESize20mm
    FlavorFRUITImprint Code capsule
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83202-1469-320 mg in 1 CAPSULE; 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(83202-1469)