Label: HCLO DISINFECTANT- hypochlorous acid liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 77263-001-01, 77263-001-02, 77263-001-03, 77263-001-04 - Packager: Suzhou HVHA Medical Technology Development Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
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 28, 2021
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Main ingredient
- Properties
- Categories of microorganism to be killed
- Application scope
-
Indication for use
1. Disinfection of hand: Spray the original solution once, take effect for 5 minutes.
2. Disinfection of air: Spray the original solution once, take effect for 20 minutes.
3. Disinfection of fabric: Spray the original solution once, take effect for 5 minutes.
4. Disinfection of surface of object: Spray the original solution once, take effect for 5 minutes.
5. Disinfection of fruit or vegetable: Spray the original solution, take effect for 5 minutes.
- Notices
- WARNINGS
-
Function mechanism
HCLO is a kind of strong oxidant and it is decomposed into nascent oxygen which is strong oxidability to makes proteins and other substances of bacteria or virus denatured and play a bactericidal effect. HCLO infiltrates into the bacteria or virus and oxidizes with organic macromolecules such as protein, nucleic acid and enzyme, and enzymes to kill the pathogenic microorganisms. The chloride ion generated from HCLO can also significantly change the osmotic pressure of bacteria or virus, making their cells lose viability and die.
- Storage
- Inactive ingredients
- Purpose
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
HCLO DISINFECTANT
hypochlorous acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77263-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID 0.1 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM SILICATE (UNII: IJF18F77L3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77263-001-01 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/03/2020 2 NDC:77263-001-02 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/03/2020 3 NDC:77263-001-03 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/03/2020 4 NDC:77263-001-04 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/03/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/03/2020 Labeler - Suzhou HVHA Medical Technology Development Co.,Ltd. (421344661) Registrant - Suzhou HVHA Medical Technology Development Co.,Ltd. (421344661) Establishment Name Address ID/FEI Business Operations Suzhou HVHA Medical Technology Development Co.,Ltd. 421344661 manufacture(77263-001)