Label: DISINFECTANT- hocl liquid

  • NDC Code(s): 82377-201-01, 82377-201-02, 82377-201-03, 82377-201-04, view more
    82377-201-05, 82377-201-06, 82377-201-07, 82377-201-08, 82377-201-09, 82377-201-10, 82377-201-11
  • Packager: Jinhua Shuxin Pharmaceutical Biotechnology 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 January 30, 2023

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

View All Sections
  • SPL UNCLASSIFIED SECTION

    Disinfectant

  • Active Ingredient(s)

    HOCLl 0.01% g/mL. Purpose: Antiseptic

  • Purpose

    Disinfectant

  • Use

    Disinfectant to help reduce bacteria that potentially can cause disease.

  • Warnings

    For external use only.

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
    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 swallowed, get medical help or contact a Poison Control Center right away.

  • STOP USE

    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

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

  • Directions

    • Spray on the skin 3-5 times each use. No rinsing reqiured.
  • Other information

    • Store between 15-30C (59-86F)
  • Inactive ingredients

    WATER

  • Package Label - Principal Display Panel

    label

  • INGREDIENTS AND APPEARANCE
    DISINFECTANT 
    hocl liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82377-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.01 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82377-201-0115 mL in 1 BOTTLE; Type 0: Not a Combination Product11/04/2021
    2NDC:82377-201-0230 mL in 1 BOTTLE; Type 0: Not a Combination Product11/04/2021
    3NDC:82377-201-0350 mL in 1 BOTTLE; Type 0: Not a Combination Product11/04/2021
    4NDC:82377-201-0460 mL in 1 BOTTLE; Type 0: Not a Combination Product11/04/2021
    5NDC:82377-201-05100 mL in 1 BOTTLE; Type 0: Not a Combination Product11/04/2021
    6NDC:82377-201-06200 mL in 1 BOTTLE; Type 0: Not a Combination Product11/04/2021
    7NDC:82377-201-07300 mL in 1 BOTTLE; Type 0: Not a Combination Product11/04/2021
    8NDC:82377-201-08500 mL in 1 BOTTLE; Type 0: Not a Combination Product11/04/2021
    9NDC:82377-201-091000 mL in 1 BOTTLE; Type 0: Not a Combination Product11/04/2021
    10NDC:82377-201-105000 mL in 1 BOTTLE; Type 0: Not a Combination Product11/04/2021
    11NDC:82377-201-1125000 mL in 1 BOTTLE; Type 0: Not a Combination Product11/04/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/04/2021
    Labeler - Jinhua Shuxin Pharmaceutical Biotechnology Co., Ltd. (541278228)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jinhua Shuxin Pharmaceutical Biotechnology Co., Ltd.541278228manufacture(82377-201)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!