11 September 1986
2 May 1986
COMMERCIAL ITEM DESCRIPTION
ASPIRIN ALUMINUM HYDROXIDE GEL, DRIED,
AND MAGNESION OXIDE TABLETS
The General Services Administration has authorized the use of this Commercial Item Description.
Shall be Aspirin, Aluminum Hydroxide Gel, Dried and Magnesium Oxide Tablets.
Shall be tablets containing 500 mg of Aspirin, 150 mg of Dried Aluminum Hydroxide Gel and 150 mg of Magnesium Oxide per tablet within the designated assay limits for the tablets.
Shall assay to contain not less than 95.0 percent and not more than 105.0 percent of the required amount of aspirin per tablet when determined by a suitable, accurate, and reproducible method.
Shall assay to contain not less than 90.0 percent and not more than 110.0 percent of the required amount of dried Aluminum Hydroxide Gel and Magnesium Oxide per tablet when determined by a suitable, accurate, and reproducible method.
Shall assay to contain not more than 3 percent free Salicylic Acid based on the labeled aspirin content per tablet when determined by a suitable, accurate, and reproducible method.
Workmanship. The tablets shall be free from defects which detract from their appearance or impair their serviceability.
Unit. Bottle (BT). One bottle containing 100 tablets, as specified, constitutes one unit. Bottle shall be supplied with a child-resistant safety closure.
DISTRIBUTION STATEMENT A: Approved for public release; distribution is unlimited.
For Parts Inquires submit RFQ to Parts Hangar, Inc.
© Copyright 2015 Integrated Publishing, Inc.
A Service Disabled Veteran Owned Small Business