Overview
Hypochlorite is an ion composed of chlorine and oxygen with the chemical formula ClO−. Being unstable in the pure form, hypochlorite is most commonly used for bleaching, disinfectation, and water treatment purposes in its salt form, sodium hypochlorite. Hypochlorite is often used as a chemical reagent for chlorination and oxidation reactions.
Indication
Indicated for over-the-counter use as a disinfectant agent in the sodium hypochlorite form.
Associated Conditions
No associated conditions information available.
Research Report
Hypochlorite (DB11123): A Comprehensive Monograph on its Chemical, Pharmacological, and Clinical Profile
I. Introduction and Overview
Hypochlorite, identified in DrugBank as DB11123, represents the active chemical moiety—the hypochlorite ion (ClO−)—that serves as the cornerstone for a class of potent, broad-spectrum antimicrobial and disinfectant agents.[1] While the formal database entry refers to this simple inorganic anion, its practical application in medicine, public health, and industry is realized almost exclusively through its salt forms, most notably aqueous solutions of sodium hypochlorite (
NaClO).[3] This report provides a multi-disciplinary analysis of hypochlorite, integrating its fundamental chemistry, its non-specific and highly effective antimicrobial pharmacology, its century-long history of clinical application in wound care and disinfection, its significant toxicological profile, and its complex, use-dependent regulatory status.
The central theme of this monograph is the inherent duality of hypochlorite: its powerful, non-specific biocidal activity is simultaneously its greatest therapeutic asset and its most significant safety liability. The chemical properties that enable it to eradicate a wide range of pathogens by indiscriminately destroying organic molecules are the very same properties that can cause severe corrosive damage to host tissues upon improper use. Consequently, nearly two centuries of scientific and medical development have been dedicated to a singular goal: harnessing its profound efficacy while mitigating its intrinsic toxicity. This endeavor has centered on the precise control of concentration, pH, formulation stability, and application technique. A critical distinction must be maintained throughout this analysis between the hypochlorite ion (ClO−), the active principle, and the formulated agents like sodium hypochlorite solution, which represent the chemical vehicle for its delivery. This distinction is not
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/08/13 | Not Applicable | Completed | Sacide Duman | ||
2025/07/02 | Not Applicable | Recruiting | ESRA DAĞCI | ||
2025/05/14 | Not Applicable | Not yet recruiting | |||
2025/02/06 | Phase 1 | Completed | Armed Forces Institute of Dentistry, Pakistan | ||
2023/08/21 | Phase 4 | Completed | |||
2023/08/03 | Phase 3 | Completed | |||
2022/04/27 | Phase 2 | UNKNOWN | |||
2022/04/01 | Phase 2 | Completed | |||
2022/03/22 | Not Applicable | Completed | |||
2021/12/07 | Phase 2 | UNKNOWN |
FDA Drug Approvals
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No FDA approvals found for this drug. |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
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No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
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No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
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No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
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No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
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No TGA approvals found for this drug. |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
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EXSEPT (0.114%) | alcavis hdc llc | 02245790 | Liquid - Topical | 0.114 % | 5/1/2002 |
R 77 DPS | dr reckeweg canada | 02095645 | Drops - Oral | 2 D / ML | 12/31/1994 |
DAKIN'S SOLUTION 0.5% MODIFIED | century pharmaceuticals inc. | 00658529 | Solution - Topical | 5 G / L | 12/31/1986 |
EXSEPT | alcavis hdc llc | 02245530 | Liquid - Topical | 0.057 % | 5/1/2002 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
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No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
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No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
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No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
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No UK EMC drug information found for this drug. |
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