Label: SSACSU HAND SANITIZER- hypochlorous acid spray

  • 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 11, 2020

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  • ACTIVE INGREDIENT

    Active ingredients: Hypochlorous Acid 0.005%

  • INACTIVE INGREDIENT

    Inactive ingredients
    Water

  • PURPOSE

    Purpose: Antiseptic

  • WARNINGS

    Warnings:

    For external use only-hands

    When using this product
    ■ Keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ Avoid contact with broken skin. ■ Do not inhale or ingest.

    Stop use and ask a doctor if skin irritation or rash develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Uses

    Uses:

    Hand sanitizer to decrease bacteria on the skin that could cause disease

  • Directions

    Directions:

    Place enough product on hands to cover all surfaces. Rub hands together until dry.
    Supervise children under 6 years of age when using this product to avoid swallowing.

  • Other information

    Other information

    Store between 0-30C (32-86F)
    Avoid freezing and excessive heat above 40C (104F)

  • QUESTIONS

    Questions?
    053-218-2511 www.multibio.co.kr

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    SSACSU HAND SANITIZER 
    hypochlorous acid spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76847-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Hypochlorous Acid (UNII: 712K4CDC10) (Hypochlorous Acid - UNII:712K4CDC10) Hypochlorous Acid0.025 g  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76847-011-01500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/01/2020
    Labeler - Multibio Co., Ltd. (693713128)
    Registrant - Multibio Co., Ltd. (693713128)
    Establishment
    NameAddressID/FEIBusiness Operations
    Multibio Co., Ltd.693713128manufacture(76847-011)
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