Label: NOW ST- 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 September 23, 2020

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

  • Active Ingredients

    Nitric oxide

  • USE

    Use it as it is or as a container.

    It is harmless to use on the human body, but do not use it as much as possible.

  • directions

    Apply an appropriate amount to the container and spray it where you want to disinfect it.

  • Keep out of reach of children

    Keep out of reach of children

  • Warnings

    Warnings

    do not use


    - in children less than 2 months of age.
    - on open skin wounds.
    - Keep away from your child.
    - Always seal and store in a container.

  • Other information


    - store between 15~30 (59~86F)
    - avoid freezing and excessive heat above 40 (104F)

  • question


    WoongBiotech Co.,Ltd 93, LS-ro 116beon-gil, Dongan-gu,
    Anyang-si, Gyeonggi-do, Korea
    +82-2-6952-6767

  • Stop use and ask doctor

    If you have swallowed it or have an allergic reaction to your skin, stop using it and consult a doctor.

  • Inactive ingredient


    purified water

  • PURPOSE

    Antimicrobial

  • label

    80519-301-01

    80519-301-01

  • INGREDIENTS AND APPEARANCE
    NOW ST 
    nitric oxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80519-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NITRIC OXIDE (UNII: 31C4KY9ESH) (NITRIC OXIDE - UNII:31C4KY9ESH) NITRIC OXIDE1.1157 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 98.843 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80519-301-0120000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/24/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/24/2020
    Labeler - WoongBiotech Co.,Ltd (695504425)
    Registrant - WoongBiotech Co.,Ltd (695504425)
    Establishment
    NameAddressID/FEIBusiness Operations
    WoongBiotech Co.,Ltd695504425manufacture(80519-301)