Tampered toxic cough syrup

I've tried numerous times to contact the United States food and drug administration forensic chemistry center in Cincinnati,Ohio the coordinator tells me that someone inside the manufacturer Bio-pharm inc. committed a serious federal crime when they tampered and chemically poisoned the assured tussin DM cough syrup product I purchased from a Dollar tree store,that left me seriously ill with permanent health affects,she says the police and food and drug administration office of criminal investigation agents where Bio-pharm inc is located went inside to pursue the person involved. The FDA has refused to give me the right to the positive chemical findings or give me the identity of the small dark amorphous particles and fibrous particle contaminants their analysts found inside the dark brown plastic bottle with a label stuck to it reading" assured Tussin DM cough syrup. I want this coordinator who gathered all of the chemical toxins information and proof of tampering to FDA OCI agents in Levittown,PA where this happened,so far every FDA lab that touched and tested this poisonous liquid refuses to speak to me. Why did the FDA freedom of information act office inside the FDA office of criminal investigations headquarters send me a letter telling me "we the FDA have deleted this information from me and the public, and the Detroit Michigan FDA office for the Indiana district ,where the FDA forensic chemistry center in Cincinnati,Ohio coordinator told me to call and they would share the names of the chemicals they also found inside this bottle with me,when I called the lab person there tells me she can't disclose the names of these chemicals that poisoned me and hung up the phone. I want anyone of those FDA people to tell me the truth ! I deserve to know what the *** is this UV fluorescent radioactive chemical compound is... besides the concentrated acid and fluorine,what is the luminating substance in this stuff ,that fluoresed inside my mouth inside a darkened x-Ray room that's caused internal bleeding inside my small intestines and inside my stomach and caused esophageal stricture ect. I want dollar tree inc and Bio-pharm inc to take responsibility for the damage their defected product is causing me !
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ID
#1099467 Review #1099467 is a subjective opinion of poster.
Reason of review
Damaged or defective
New Reviewer

Government/FDA banned Clove cigarettes

For those Clove smokers out there that are still as outraged as I am about the ban...., I have some information that was sent to me. If you feel the need as I did to write them and tell them how stupid our governments thinking is on the Clove ban, this will give you some new information. Thanks,B. Wuertenberg WARNING LETTER The Food and Drug Administration (FDA) reviewed your website at http://www.clovecigaretteshop.com. on October 6, 2009, and determined that your website has been offering for sale Absolute Mild, Bentoel Class Mild, Djarum Black, Djarum Coklat, Forum Special 12 Kretek, Gudang Garam Signature Red 20, Djarum Black Tea, Adobijang 12 Kretek, Bentoel Star Mild, Djarum Black Cappuccino, Djarum LA Lights, GG Surya Slimz 16 White Edition, Gudang Garam Signature Mild, Lodjie 12 Kretek, Marlboro Filter Kretek Mix 9, Neo Mild, Rod's Mild, Sampoerna A Mild, Sampoerna Avolution Mild, Sampoerna Dijsamsoe 234 Magnum, Sampoerna Dijsamose 234, Sukun Orange Kretek, and Tali Jagat Kretek (referred to hereafter as flavored cigarette products) to consumers in the United States, Under section 201 (rr) of the FederalFood, Drug, and Cosmetic Act (FFDCA), as amended by the Family Smoking Prevention and Tobacco Control Act (FSPTCA), 21 U.S.C. § 321 (rr), these products are tobacco products because they are made or derived from tobacco and intended for human consumption. According to the information and materials on your website we reviewed, your products listed above are represented as cigarettes that contain artificial or natural flavors that are characterizing flavors of the products and, as such, are adulterated and/or misbranded. Section 907(a)(1)(A) of the FFDCA, 21 U.S.C. § 387g(a)(1)(A), provides, as part of the tobacco product standards, a "special rule for cigarettes"as follows: [A] cigarette or any of its component parts (including the tobacco, filter, or paper) shall not contain, as a constituent (including a smoke constituent) or additive, an artificial or natural flavor (other than tobacco or menthol) or an herb or spice, including strawberry, grape,orange, clove, cinnamon, pineapple, vanilla, coconut, licorice, cocoa, chocolate, cherry, or coffee, that is a characterizing flavor of the tobacco product or tobacco smoke. After the September 22, 2009 effective date for this provision, flavored cigarettes marketed and sold in the United States in violation of this provision are adulterated under section 902(5) of the FFDCA, 21 U.S.C. § 387b(5). Your website represents that the above-listed products are cigarettes and contain clove, tea, cappuccino, or orange that are characterizing flavors of the tobacco products, If your above-listed flavored cigarette products contain clove, tea, cappuccino, or orange that are characterizing flavors of the tobacco products, your products are adulterated under section 902(5) of the FFDCA, 21 U.S.C. § 387b(5), because they are represented as cigarettes and fail to comply with the special rule for cigarettes detailed in section 907(a)(1)(A) of the FFDCA, 21 U.S.C. § 387g(a)(1)(A). If, however, your products do not contain a flavor, herb, or spice that is a characterizing flavor of the tobacco products, they are misbranded under section 903(a)(1) of the FFDCA, 21 U.S.C. § 387c(a)(1), as their labeling is false and misleading because it makes the representation that the products contain clove, tea, cappuccino, or orange that is a characterizing flavor of the tobacco product. You should immediately correct this violation by ceasing the marketing and sale of your products or taking other appropriate action to bring your products into compliance with the requirements of the FFDCA Failure to correct this violation may result in regulatory action being initiated by the FDA without further notice. These actions may include, but are not limited to, seizure and injunction. As you are not located in the United States, please note that adulterated or misbranded tobacco products offered for importation into the United States are subject to detention and refusal of admission. We will advise the appropriate regulatory or law enforcement officials in the country from which you operate that FDA considers your products listed above to be adulterated and/or misbranded products that cannot be legally sold to consumers in the United States. Please submit a written response to this letter within 15 working days from the date you receive this letter, describing your intent to comply with this request and explaining your plan for discontinuing the marketing and sale, or relabeling, of these tobacco products. Please direct your response to Ann Simoneau, Regulatory Counsel, Center for Tobacco Products, Food and Drug Administration, 9200 Corporate Boulevard, Rockville, Maryland 20850, or send via email to FDAFlavoredCigaretteTaskForce@***.GOV. We remind you that only written communications are considered official. The violation discussed in this letter does not necessarily constitute an exhaustive list. It is your responsibility to ensure that your tobacco products comply with the applicable provisions of the FFDCA, as amended by the FSPTCA, that are currently in effect. Sincerely, /s/ Lawrence R. Dayton, M.S.P.H., M.D. Director, Center for Tobacco Products
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ID
#162145 Review #162145 is a subjective opinion of poster.
Location
Reston, Virginia

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Food and Drug Administration is an official web site of Department of Health and Human services in America. All actions of this governmental department are aimed to provide residents of the USA with quality basic human services. At this portal you will find information about drugs, food, cosmetic products,vaccination for pets, tobacco products, medical devices and so on. This consumer protection agency was established in April 11, 1953. The headquarter is in Silver Spring, MD. Browsing this portal, all consumers can find many answers on their questions and become protected when it comes about manufactured food and medical products.

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