We all have read the assertion by the FDA that the Carts they tested had trace amounts of ethylene glycol.
Are E cigarettes falsely being accused of using adulterated materials? Probably not. Anyone who uses USP glycol may well be introducing small amounts into their products. Apparently USP recognizes trace ethylene glycol adulteration is a problem with current Propylene Glycol standards and has modified the testing.
Could this mean the dreaded "poisonous antifreeze" is in massive amounts of consumer products? Probably so...
The sky is indeed falling
Are E cigarettes falsely being accused of using adulterated materials? Probably not. Anyone who uses USP glycol may well be introducing small amounts into their products. Apparently USP recognizes trace ethylene glycol adulteration is a problem with current Propylene Glycol standards and has modified the testing.
Could this mean the dreaded "poisonous antifreeze" is in massive amounts of consumer products? Probably so...
The sky is indeed falling
USP Revises Five High-Priority Pharmaceutical Excipient Monographs: Propylene Glycol, Sorbitol Solution, Sorbitol Sorbitan Solution, Noncrystallizing Sorbitol Solution, and Maltitol Solution
Updated: April 30, 2010
Based on a request from of the Food and Drug Administration (FDA) in February, 2009, USP has revised and strengthened its monographs for five pharmaceutical excipients used in drug formulations-Propylene Glycol, Sorbitol Solution, Sorbitol Sorbitan Solution, Noncrystallizing Sorbitol Solution, and Maltitol Solution. These efforts are to assist in preventing future diethylene glycol (DEG) and ethylene glycol (EG) adulteration.
The proposed revisions to the above-named monographs include limits for DEG and EG, each at a level of not more than 0.10 percent in the Identification test. These revisions are consistent with the recent USP Glycerin monograph revision to help prevent future episodes of pharmaceutical adulterations with these poisonous chemicals.
Hot Topics: USP Propylene Glycol and Sorbitol Solution InformationUpdated: April 30, 2010
Based on a request from of the Food and Drug Administration (FDA) in February, 2009, USP has revised and strengthened its monographs for five pharmaceutical excipients used in drug formulations-Propylene Glycol, Sorbitol Solution, Sorbitol Sorbitan Solution, Noncrystallizing Sorbitol Solution, and Maltitol Solution. These efforts are to assist in preventing future diethylene glycol (DEG) and ethylene glycol (EG) adulteration.
The proposed revisions to the above-named monographs include limits for DEG and EG, each at a level of not more than 0.10 percent in the Identification test. These revisions are consistent with the recent USP Glycerin monograph revision to help prevent future episodes of pharmaceutical adulterations with these poisonous chemicals.