Label: INCARE ALL IN ONE PLUS- hypochlorous acid liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated January 11, 2022

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  • Active Ingredient(s)

    Hypochlorous Acid 0.004%

  • Purpose

    Antibiotic (Sanitize)

  • Use(s)

    Disinfectants - General use (for general objects, air conditioner, drainpipes, and mold removal) handbag, Furniture, etc.

    Deodorizing agents - General use (for indoor space and objects) and automotive (for real life), bathroom, toilet, clothes, etc.

    Cleaners - General use (bathrooms, toilets, carpets, washing tanks drains, building floors, shoes, furniture, musical instruments), motor vehicles (real content)

  • Warnings

    Do not use it for any other purpose.

  • Warnings

    Do not mix with water or other chemicals.

    Do not spary directly on electrical and electronic products.

  • Warnings

    Keep out of reach of children.

  • Warnings

    If you drink the solution, drink enough water and consult your doctor.

    Stop use and ask a Doctor: If skin problems occur during use, discontinue the use immediately.

  • Directions

    Spray enough solution at the place where you want to sterilize.

    Natural drying is recommended after spraying.

  • Other Information

    Store between 15-30C (59-86F)

  • Inactive Ingredient

    Water

  • Package Label

    500ml NDC: 77162-201-01 Label

    500ml NDC: 77162-201-01 Label Box

    20000ml NDC: 77162-201-02 Label

  • INGREDIENTS AND APPEARANCE
    INCARE ALL IN ONE PLUS 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77162-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.004 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 99.996 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77162-201-01500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/10/2020
    2NDC:77162-201-0220000 mL in 1 BOTTLE; Type 0: Not a Combination Product07/03/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/10/2020
    Labeler - MCCBIO CO., LTD (695801342)
    Registrant - MCCBIO CO., LTD (695801342)
    Establishment
    NameAddressID/FEIBusiness Operations
    MCCBIO CO., LTD695801342manufacture(77162-201)
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