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Standard Guide for Evaluation of Residual Effectiveness of Antibacterial Personal Cleansing Products

ASTM E2752-25

Organization:
ASTM - ASTM International
Year: 2025

Abstract: 5.1 The procedure is used to evaluate personal cleansing products containing antibacterial ingredients that are intended to reduce the number of organisms on intact skin. It also may be used to demonstrate the effect of residual antibacterial activity by means of inhibition of the proliferation of bacteria on the skin after contact.
URI: http://yse.yabesh.ir/std/handle/yse/343981
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    Standard Guide for Evaluation of Residual Effectiveness of Antibacterial Personal Cleansing Products

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contributor authorASTM - ASTM International
date accessioned2025-09-30T19:30:34Z
date available2025-09-30T19:30:34Z
date copyright2025
date issued2025
identifier othere2752-25.pdf
identifier urihttp://yse.yabesh.ir/std/handle/yse/343981
description abstract5.1 The procedure is used to evaluate personal cleansing products containing antibacterial ingredients that are intended to reduce the number of organisms on intact skin. It also may be used to demonstrate the effect of residual antibacterial activity by means of inhibition of the proliferation of bacteria on the skin after contact.
languageEnglish
titleStandard Guide for Evaluation of Residual Effectiveness of Antibacterial Personal Cleansing Productsen
titleASTM E2752-25num
typestandard
statusActive
treeASTM - ASTM International:;2025
contenttypefulltext
scope1.1 This guide is designed to demonstrate the effectiveness of an antibacterial personal cleansing product in reducing the numbers of a marker organism (representing transients) both immediately and after prolonged exposure to (cleansing) washing when used as recommended under simulated use conditions. The method demonstrates the effect of residual antibacterial activity by means of inhibition of proliferation of bacteria on the skin after the contact period. Antimicrobial activity is compared with a vehicle or to a baseline organism count. 1.2 A knowledge of microbiological techniques is required for these procedures. 1.3 Performance of this procedure requires the knowledge of regulations pertaining to the protection of human subjects (21 CFR Parts 50 and 56). 1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.5 This standard may involve hazardous materials, operations, and equipment. This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. 1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
identifier DOI10.1520/E2752-25
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