A neutralizer system was developed and validated for use in the in vitro bactericidal evaluation of three commonly used antiseptics, namely, Hibiclens (4% [wt/vol] chlorhexidine gluconate), Betadine (7.5% [wt/vol] povidone-iodine), and pHisoHex (3% [wt/vol] hexachlorophene). The neutralizer finally selected after a screening of 12 potential candidates consisted of 3% Asolectin, 10% Tween 80, and 0.3% sodium thiosulfate in diluent, and 0.3% Asolectin, 1% Tween 80, and 0.3% sodium thiosulfate in the recovery agar. This neutralizer system was tested and validated for its neutralizing capacity for the three antiseptics, as well as for its lack of inherent bactericidal action against Staphylococcus aureus and a number of gram-negative bacteria of clinical significance. With no more than a 10-fold dilution of the antiseptic, the selected neutralizer system was 100% effective in neutralizing all the bacteriostatic carry-over of the three antiseptics and was also completely without any inherent bactericidal action against all the test organisms used. Sodium sulfite (considered to be a potential inactivator for iodophores such as Betadine), even in concentrations as low as 0.1%, was found to be ineffective or inherently bactericidal, whereas 0.3% sodium thiosulfate, in combination with Asolectin and Tween 80, was adequate (effective as well as nonbactericidal) and was considered to be essential for the neutralization of the three test antiseptics, namely, Hibiclens, Betadine, and pHisoHex.Chemical agents commonly known as inactivators or neutralizers are often used for (i) the bactericidal evaluation of antimicrobial agents, antiseptics, and disinfectants; (ii) the evaluation of preservative efficacy in many pharmaceuticals, toiletries, and cosmetic products; and (iii) the microbial limit testing ofproducts containing antimicrobial agents. The need for an adequate neutralizer in some of these applications is well documented and rightfully stressed (2-4, 11-14). The selected neutralizer should not only be able to completely inactivate all of the bacteriostatic activity of the residual antimicrobial agent likely to be carried over into recovery media, but also be inherently non-bactericidal to the test organisms (4).As