News & Events

FDA PRESS STATEMENT

For Immediate Release: Tuesday, March 6, 2012
Media Inquiries: FDA Office of Media Affairs, 301-796-4540, fdaoma@fda.hhs.gov
Trade Press Inquiries: Sebastian Cianci, 240-402-2291, sebastian.cianci@fda.hhs.gov
Consumer Inquiries: 888-INFO-FDA
 

FDA issues warning letter to makers of AeroShot “caffeine inhaler”

 
The U.S. Food and Drug Administration today issued a warning letter to Breathable Foods Inc., makers of AeroShot, for false or misleading statements in the labeling of their product, and told the company that the Agency has questions about the safety of the “caffeine inhaler.” The FDA also expressed concern about the use of AeroShot by children and adolescents and in combination with alcohol.
 
The company claims AeroShot is designed to provide “breathable energy, anytime, anyplace.” The company also claims on its website that its product is intended to be ingested by swallowing.  The company’s labeling is false or misleading because these two claims contradict each other. A product cannot be intended for both inhalation and ingestion because the functioning of the epiglottis in the throat keeps the processes of inhaling and swallowing separate.      
 
FDA is also concerned about AeroShot’s safety because label statements such as “breathable energy” may confuse consumers about the proper use of AeroShot and encourage them to try to inhale it into their lungs. Caffeine is not normally inhaled into the lungs and the safety of doing so has not been well studied.  While the company claims on its website that decades of research have established that the particles in AeroShot are too big to enter the lungs, the company does not point to any specific research in support of this claim.
 
In addition, the company’s website indicates that AeroShot is “not recommended for those under 18 years of age,” and the product label states that it is “not intended for people under 12.” But the website also appears to target these age groups by suggesting it be used when studying.
 
The AeroShot website also includes links to news articles and videos that refer to use of the product in conjunction with drinking alcohol.  Although these news items do not advocate taking AeroShot while drinking alcohol and express health concerns about such use, the presence of the news items on the AeroShot promotional website publicizes and therefore may encourage the use of AeroShot with alcohol. While using caffeine when drinking may lead consumers to feel “less drunk,” it does not reduce blood alcohol levels.
 
FDA regulations require manufacturers to ensure that a product is safe and properly labeled before being brought to market. FDA has instructed Breathable Foods Inc. to correct the violations cited in the warning letter and provide information on research the company cites so the agency can evaluate the research. The company has 15 business days to respond to the agency with a plan to bring the product into compliance with FDA regulations.
 
The warning letter also charges that the product label does not include contact information for consumers to report any adverse events to the company, as required under federal law. Consumers who believe they have suffered illness or injury from using AeroShot should also report those events to their regional FDA Consumer Complaint Coordinators. The agency also encourages healthcare providers to report to FDA any adverse events in their patients that are associated with AeroShot. As of March 6, 2012, FDA has not received any adverse event reports associated with the product.
 
FDA’s first priority is always to ensure the health of consumers. The agency takes very seriously any health problems that may be caused by products it regulates. The FDA will review any information brought to the agency’s attention about this product and will consider regulatory action if a violation of the Federal Food, Drug and Cosmetic Act has occurred.  
 
For more information:
 
AeroShot Warning Letter:
 
How FDA regulates dietary supplements:
 
Report a complaint to your regional Consumer Complaint Coordinator:
 
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The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.
 
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