Label: DAILY DOCTOR HYPOCHLOROUS ACID DISINFECTANT LIQUID- hypochlorous acid spray

  • NDC Code(s): 76836-002-01, 76836-002-02
  • Packager: GFC Life Science Co., Ltd.
  • 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 May 14, 2020

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  • Active ingredient

    HYPOCHLOROUS ACID 0.1%

  • Purpose

    Antimicrobial

  • Use

    • Prevent and treat infection of the skin
  • Warnings

    For external use only

    Do not use if sensitive of chlorine compounds.

    Stop use and ask a doctor if redness, irritation or swelling or pain persists or increases.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Use as liquid. Sterilize by immersing completely for about 3 to 5 minutes. For instruments that are difficult to deposit, spray and sterilize for about 3 minutes before wiping off.
  • Inactive ingredients

    Water, Hydrochloric acid

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    DAILY DOCTOR HYPOCHLOROUS ACID DISINFECTANT LIQUID 
    hypochlorous acid spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76836-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLORITE ION - UNII:T5UM7HB19N) HYPOCHLOROUS ACID0.0001 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76836-002-0160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/14/2020
    2NDC:76836-002-02500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/14/2020
    Labeler - GFC Life Science Co., Ltd. (688325518)
    Registrant - GFC Life Science Co., Ltd. (688325518)
    Establishment
    NameAddressID/FEIBusiness Operations
    GFC Life Science Co., Ltd.688325518manufacture(76836-002)