Label: BRILLE BRILLE STERILIZING WATER MIST- hypochlorous acid 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 July 8, 2021

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

  • Active ingredient[s]

    Hypochlorous acid

  • Purpose

    Sterilizing

  • Use[s]

    Face and hand sterilizer to help reduce various bacteria that may can cause disease. For use when soap or any alien material are not available

  • Warning[s]

    Keep away from heat or flame

  • Do not use

    In children less than 10 months age and forbid lime water or your own serum.

  • When using this product

    usable on eyes, ears, and mouth

  • Stop use and ask a doctor

    if irritation or rash occurs, These may be signs of a serious condition.

  • Keep out of reach of children

    if the child has any allergy, it may cause any allergic disease in this case, please get medical help.

  • Directions


    -Place enough product on skin and hands to cover all surfaces,
    -Please avoid children to use it.

  • Other information


    -Store between 5~35C (41~95F)
    -Avoid freezing and excessive heat above 40C (104F)

  • Inactive ingredients

    Water

  • Package Label

    81546-301-01

  • INGREDIENTS AND APPEARANCE
    BRILLE BRILLE STERILIZING WATER MIST 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81546-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID8 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81546-301-0130 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/05/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/05/2021
    Labeler - Beauhealline Co., Ltd (694784706)
    Registrant - Beauhealline Co., Ltd (694784706)
    Establishment
    NameAddressID/FEIBusiness Operations
    Beauhealline Co., Ltd694784706manufacture(81546-301)