26 March 1987
INTERIM COMMERCIAL ITEM DESCRIPTION
ANTISEPTIC-ANESTHETIC SOLUTION, PHENOLATED
The General Services Administration has authorized the use of this Interim Commercial Item Description which was developed by the Defense Personnel Support Center, Directorate of Medical Materiel, DPSC-RST, 2800 South 20th Street, Philadelphia, PA 19101, based upon currently available technical information.
Shall be a flavored, clear, non-irritating, aqueous antiseptic-anesthetic solution containing Phenol or Phenolated compound and other inactive ingredients such as flavors, sweetners, dyes and other ingredients approved by the FDA for internal use.
The antiseptic-anesthetic solution shall be suitable for use as a sore throat spray that may be swallowed and suitable as a gargle/rinse and mouthwash when use according to approved FDA labeled directions.
Shall contain a total phenol content of not less than 1.26 percent w/v and not more than 1.54 percent w/v.
The presence of all of the ingredients in the formula for the solution shall be determined from the batch formulation sheet as kept on file by the manufacturer.
The bidder or offeror shall submit with its bid or proposal the test methods and results for the phenol assay and any other physical or chemical testing protocols approved by the FDA.
Such methods shall be employed in the testing of the solution and need not be resubmitted provided the bidder or offeror certifies that there has been no change in formulation or method of manufacture.
Materials used in the manufacture of the solution shall be of pharmaceutical grade.
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
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