Label: HYPOCHLOROUS ACID liquid

  • Contains inactivated NDC Code(s)
    NDC Code(s):     78295-007-01, 78295-007-02, 78295-007-03, 78295-007-04, view more
    78295-007-05, 78295-007-06, 78295-007-07, 78295-007-08, 78295-007-09, 78295-007-10, 78295-007-11, 78295-007-12, 78295-007-13, 78295-007-14
  • Packager: GUANGZHOU YIQI TECHNOLOGY 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 December 15, 2020

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  • Active ingredient

    ActiveIngredient：Hypochlorous Acid(0.02%)

  • ​Purpose

    Purpose：Antimicrobial

  • Usage

    Application

    Effective content, ppm

    Dilution ratio

    Usage mode

    TIME

    Object Surface

    40ppm

    1:4

    Spray and wipe

    10minutes

    The Air

    33ppm

    1:5

    Spray

    10minutes

    Fruits Vegetables Seafood

    40ppm

    1:4

    Spray, wipe or soak

    10minutes

    Fabric

    40ppm

    1:4

    Spray

    10minutes

  • WARNINGS

    [WARNINGS]
    For external use only.
    Electricshock equipment should be prevented.

  • DO NOT USE

    /

  • When using this product

    [When using this product]
    When spraying it within a space， high humidity which could cause short circuit to electrical equipment.

  • STOP USE

    /

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    [Directions]
    Children under 6 years of age should be supervised when using this product.
    Keep away from sunlight and heat.

  • Other information

    [Other information]
    Store below 106F.(41℃)
    The effective sterilization concentration of slightly acidic hypochlorous acidis30PPm-50PPm， high concentration use should be avoided as far as possible.

  • Inactive ingredient

    Inactive ingredient：
    water 99.98%

  • Package Label - Principal Display Panel

    78295-007-01 0.1L78295-007-02 0.25L78295-007-03 0.5L78295-007-04 0.71L78295-007-05 1L78295-007-06 4L78295-007-07 5L78295-007-07 5L78295-007-08 10L78295-007-09 18.93L78295-007-10 20L78295-007-11 25L78295-007-12 37.9L78295-007-13 208.2L78295-007-14 1000L

  • INGREDIENTS AND APPEARANCE
    HYPOCHLOROUS ACID 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78295-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.02 kg  in 100 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78295-007-040.71 L in 1 BOTTLE; Type 0: Not a Combination Product05/18/2020
    2NDC:78295-007-020.25 L in 1 BOTTLE; Type 0: Not a Combination Product05/18/2020
    3NDC:78295-007-051 L in 1 BOTTLE; Type 0: Not a Combination Product05/18/2020
    4NDC:78295-007-064 L in 1 BOTTLE; Type 0: Not a Combination Product05/18/2020
    5NDC:78295-007-030.5 L in 1 BOTTLE; Type 0: Not a Combination Product05/18/2020
    6NDC:78295-007-010.1 L in 1 BOTTLE; Type 0: Not a Combination Product05/18/2020
    7NDC:78295-007-0810 L in 1 BOTTLE; Type 0: Not a Combination Product05/18/2020
    8NDC:78295-007-0918.93 L in 1 DRUM; Type 0: Not a Combination Product05/18/2020
    9NDC:78295-007-1125 L in 1 DRUM; Type 0: Not a Combination Product05/18/2020
    10NDC:78295-007-1020 L in 1 DRUM; Type 0: Not a Combination Product05/18/2020
    11NDC:78295-007-1237.9 L in 1 DRUM; Type 0: Not a Combination Product05/18/2020
    12NDC:78295-007-075 L in 1 BOTTLE; Type 0: Not a Combination Product05/18/2020
    13NDC:78295-007-141000 L in 1 DRUM; Type 0: Not a Combination Product05/18/2020
    14NDC:78295-007-13208.2 L in 1 DRUM; Type 0: Not a Combination Product05/18/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/18/2020
    Labeler - GUANGZHOU YIQI TECHNOLOGY CO.,LTD (544707398)
    Registrant - GUANGZHOU YIQI TECHNOLOGY CO.,LTD (544707398)
    Establishment
    NameAddressID/FEIBusiness Operations
    GUANGZHOU YIQI TECHNOLOGY CO.,LTD544707398manufacture(78295-007)
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