USPlabs Jack3d
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diluted
Üye
Önemli:
FDA, 1.3 dimethylamylamine'i yasaklı maddeler listesine ekledi.Jack3d'in kimilerine göre efsanevi üstünlüğünü sağlayan şey yani.Dikkat ettiyseniz bodybuilding.com gibi siteler bile satmıyor artık.Yeni, 1.3'süz formül çıktığı an satışına devam edilecek.Sadece jack3d değil,diğer 1.3 içeren ürünler de piyasadan şimdilik çekildi.O ölüm haberleri vs'e sebep olan madde de buydu ama.Yani tamam 1.3=güç ama kontrolsüz güç.
FDA, 1.3 dimethylamylamine'i yasaklı maddeler listesine ekledi.Jack3d'in kimilerine göre efsanevi üstünlüğünü sağlayan şey yani.Dikkat ettiyseniz bodybuilding.com gibi siteler bile satmıyor artık.Yeni, 1.3'süz formül çıktığı an satışına devam edilecek.Sadece jack3d değil,diğer 1.3 içeren ürünler de piyasadan şimdilik çekildi.O ölüm haberleri vs'e sebep olan madde de buydu ama.Yani tamam 1.3=güç ama kontrolsüz güç.
hakankabaoglu
Üye
vay be hakkaten bodybuilding.com dan kaldırılmıs jack 3d,nutrex hemorage vs
3 kutu bu ürünü kullanmış biri olarak herhangi bir yan etki görmedim. 2 ölçek olmak üzere haftada 5 defa kullandım. Etkisi tartışılmaz bir ürün. Nox ürünleri bünyeden bünyeye değişiyor ama ne anımal pump ne gaspari superpump ne de bsn no xplode bunun gibi etki vermedi. Sadece alın ve deneyin.
harbiden hicbiryerde bulamiyorum boyle bilincsiz kullanan insanlar yuzunden boyle guzel urunlerden faydalanamiyoruz allah kahretsin :/
/edit
neyseki arastirmam sonucu bir sitede buldum
katılıyorum. insanlar enerji içeceğini bile doğru düzgün içmeyi beceremeyip ölüyorlar maalesef. e o zaman enerji içecekleri ve daha bir çok şeyde mi kalksın piyasadan? kaldı ki üretici firmalar gerekli uyarıları titizlikle yapıyorlar.
selim4141
Üye
Çok doğru söylüyorsun redbull içip sapıtanları biliyorum, o zaman herşey yasaklansın kafa_
kımı arkadas hoslanmıo ama bence guzel 
ataberkim
Üye
jack3d Nisan ayi sonu itibari ile Amerika'da satisi yasaklanmistir....Icindeki DMAA maddesi yuzunden... Bununla birlikte asagidaki urunler de dahil... Limitleri sinirin da bir jack3d kullanici olarak uzuldum....
FDA NEWS RELEASE
For Immediate Release: April 27, 2012
Media Inquiries: Tamara Ward, 301-796-7567, [email protected]
Trade Press Inquiries: Sebastian Cianci, 240-402-2291, [email protected]
Consumer Inquiries: 888-INFO-FDA
FDA challenges marketing of DMAA products for lack of safety evidence
Agency cites ten companies in warning letters
The U.S. Food and Drug Administration today issued warning letters to ten manufacturers and distributors of dietary supplements containing dimethylamylamine, more popularly known as DMAA, for marketing products for which evidence of the safety of the product had not been submitted to FDA.
Also referred to as 1,3-dimethylamylamine, methylhexanamine, or geranium extract, the ingredient is in dietary supplements and is often touted as a "natural" stimulant.
The companies receiving warning letters and their product names are:
Company Product(s)
Exclusive Supplements Biorhythm SSIN Juice
Fahrenheit Nutrition Lean Efx
Gaspari Nutrition Spirodex
iSatori Global Technologies, LLC PWR
Muscle Warfare, Inc. Napalm
MuscleMeds Performance Technologies Code Red
Nutrex Research Hemo Rage Black
Lipo-6 Black Ultra Concentrate
Lipo-6 Black
Lipo-6 Black Hers Ultra Concentrate
Lipo-6 Black Hers
SEI Pharmaceuticals MethylHex 4,2
SNI LLC Nitric Blast
USP Labs, LLC Oxy Elite Pro
Jack3D
"Before marketing products containing DMAA, manufacturers and distributors have a responsibility under the law to provide evidence of the safety of their products. They havent done that and that makes the products adulterated," said Daniel Fabricant, Ph.D., Director of FDAs Dietary Supplement Program.
Specifically, the warning letters cite the companies for marketing products for which a notification had not been submitted for the use of DMAA as a New Dietary Ingredient (NDI). Under current law, dietary supplement manufacturers or distributors who use certain dietary ingredients not marketed in a dietary supplement prior to October 15, 1994, are responsible for notifying the FDA of evidence to support their conclusion that their dietary supplements containing NDIs are safe. Manufacturers or distributors must submit notification at least 75 days before marketing their products. The companies warned today were marketing products for which this requirement had not been met.
The FDA warning letters also advised the companies that the agency is not aware of evidence or history of use to indicate that DMAA is safe. Under the Dietary Supplement Health and Education Act of 1994 (DSHEA), manufacturers, marketers and distributors of dietary supplements are responsible for ensuring that they are marketing a safe product.
The FDA letters noted that DMAA is known to narrow the blood vessels and arteries, which can elevate blood pressure and may lead to cardiovascular events ranging from shortness of breath and tightening in the chest to heart attack. The agency has received 42 adverse event reports on products containing DMAA. While the complaints do not establish that DMAA was the cause of the incidents, some of the reports have included cardiac disorders, nervous system disorders, psychiatric disorders, and death.
The agency additionally warned the companies that synthetically-produced DMAA is not a dietary ingredient and, therefore, is not eligible to be used as an active ingredient in a dietary supplement. DSHEA defines a dietary ingredient as a vitamin, mineral, amino acid, herb or other botanical, a dietary substance for use by man to supplement the diet, or a concentrate, metabolite, constituent, extract, or combination of these substances.
The companies have 15 business days to respond to the FDA with the specific steps they will take to address the issues in the warning letters.
For more information:
How dietary supplements are regulated
Dietary Supplement Health and Education Act of 1994
New Dietary Ingredient notification process
Reporting adverse events associated with FDA regulated products
#
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 nations food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.
Read our Blog: FDA Voice
Visit the FDA on Facebook , Flickr , YouTube and Twitter
RSS Feed for FDA News Releases
FDA NEWS RELEASE
For Immediate Release: April 27, 2012
Media Inquiries: Tamara Ward, 301-796-7567, [email protected]
Trade Press Inquiries: Sebastian Cianci, 240-402-2291, [email protected]
Consumer Inquiries: 888-INFO-FDA
FDA challenges marketing of DMAA products for lack of safety evidence
Agency cites ten companies in warning letters
The U.S. Food and Drug Administration today issued warning letters to ten manufacturers and distributors of dietary supplements containing dimethylamylamine, more popularly known as DMAA, for marketing products for which evidence of the safety of the product had not been submitted to FDA.
Also referred to as 1,3-dimethylamylamine, methylhexanamine, or geranium extract, the ingredient is in dietary supplements and is often touted as a "natural" stimulant.
The companies receiving warning letters and their product names are:
Company Product(s)
Exclusive Supplements Biorhythm SSIN Juice
Fahrenheit Nutrition Lean Efx
Gaspari Nutrition Spirodex
iSatori Global Technologies, LLC PWR
Muscle Warfare, Inc. Napalm
MuscleMeds Performance Technologies Code Red
Nutrex Research Hemo Rage Black
Lipo-6 Black Ultra Concentrate
Lipo-6 Black
Lipo-6 Black Hers Ultra Concentrate
Lipo-6 Black Hers
SEI Pharmaceuticals MethylHex 4,2
SNI LLC Nitric Blast
USP Labs, LLC Oxy Elite Pro
Jack3D
"Before marketing products containing DMAA, manufacturers and distributors have a responsibility under the law to provide evidence of the safety of their products. They havent done that and that makes the products adulterated," said Daniel Fabricant, Ph.D., Director of FDAs Dietary Supplement Program.
Specifically, the warning letters cite the companies for marketing products for which a notification had not been submitted for the use of DMAA as a New Dietary Ingredient (NDI). Under current law, dietary supplement manufacturers or distributors who use certain dietary ingredients not marketed in a dietary supplement prior to October 15, 1994, are responsible for notifying the FDA of evidence to support their conclusion that their dietary supplements containing NDIs are safe. Manufacturers or distributors must submit notification at least 75 days before marketing their products. The companies warned today were marketing products for which this requirement had not been met.
The FDA warning letters also advised the companies that the agency is not aware of evidence or history of use to indicate that DMAA is safe. Under the Dietary Supplement Health and Education Act of 1994 (DSHEA), manufacturers, marketers and distributors of dietary supplements are responsible for ensuring that they are marketing a safe product.
The FDA letters noted that DMAA is known to narrow the blood vessels and arteries, which can elevate blood pressure and may lead to cardiovascular events ranging from shortness of breath and tightening in the chest to heart attack. The agency has received 42 adverse event reports on products containing DMAA. While the complaints do not establish that DMAA was the cause of the incidents, some of the reports have included cardiac disorders, nervous system disorders, psychiatric disorders, and death.
The agency additionally warned the companies that synthetically-produced DMAA is not a dietary ingredient and, therefore, is not eligible to be used as an active ingredient in a dietary supplement. DSHEA defines a dietary ingredient as a vitamin, mineral, amino acid, herb or other botanical, a dietary substance for use by man to supplement the diet, or a concentrate, metabolite, constituent, extract, or combination of these substances.
The companies have 15 business days to respond to the FDA with the specific steps they will take to address the issues in the warning letters.
For more information:
How dietary supplements are regulated
Dietary Supplement Health and Education Act of 1994
New Dietary Ingredient notification process
Reporting adverse events associated with FDA regulated products
#
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 nations food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.
Read our Blog: FDA Voice
Visit the FDA on Facebook , Flickr , YouTube and Twitter
RSS Feed for FDA News Releases
diluted
Üye
Eger 1.3'un doping oldugunu biliyorsaniz, eminim ki ingilizceniz belirli bir seviyededir.Lutfen yabanci forumlari(tercihen bodybuilding.com'un kendi forumlarini) derinlemesine arastiriniz bu konuda.
Maddenin yasaklanmasina gelince, eger sadece jack3d yasaklanmis olsa, hadi beyler jack3d artik oldu baska markalara goc etme zamani derdim ama durum oyle degil.Cogu vg'ci tarafindan kutsal madde olarak gorunan bir icerik maddesi yasaklandi.Jack3d ile birlikte, icinde 1.3 olan urunleri bulmak su an abd'de bile gercekten zor.Jack3d'in o meshur etkisini tecrube etmek isteyenler elini cabuk tutsun cunku 1.3'lu formulun uretimi durduruldu.Su an saticilarin ellerindeki stok eridigi an pre supp'larinda bir donem kapanacak.
Ünkut
Üye
hocam amerikada yasaklandiysa avrupada neden hala yasaklanmadi ozaman? almanya böyle seylerde cok titizdir zamaninda hydroxycut i felan hemen yasakladilar fakat jack3d her shopta mevcut ve stoklarda.. ayrica hollanda shoplarindan 1,3 dimethylamylamine isimli maddeyi direk temin edebilirsiniz maddenin kullanimi ve satisi yasak degil sadece müsabakalarda kullanmak yasak.. linkleri buraya koymam ama özelden verebilirim istiyorsaniz
insanlari yanlis bilgilendirmeyelim..
Son düzenleme:
Kaanrlz
Üye
D.Y
Üye
Bu urunu sadece protein tozu kullandigim bir zaman kullanmisdim benim izlenimim antrenman sirasinda iyi bir enerji verdigi,gucu hatri sayilir bir sekilde arttirdigi(uzun sure kullanimlarda oyle hemen guc artisi beklemeyin) ve yorgunlugu azalttigi yonunde.No xplodeden daha basarili bir urun sadece tadi kötu oda 200 300 ml bise oldugu icin 1 2 dikisde bitiyor,bence bu urunu mutlaka denemelisiniz
diluted
Üye
hocam amerikada yasaklandiysa avrupada neden hala yasaklanmadi ozaman? almanya böyle seylerde cok titizdir zamaninda hydroxycut i felan hemen yasakladilar fakat jack3d her shopta mevcut ve stoklarda.. ayrica hollanda shoplarindan 1,3 dimethylamylamine isimli maddeyi direk temin edebilirsiniz maddenin kullanimi ve satisi yasak degil sadece müsabakalarda kullanmak yasak.. linkleri buraya koymam ama özelden verebilirim istiyorsaniz
FDA amerikan hukumetine bagli bir kurulustur.Verdigi kararlar sadece ABD ve bagli adalari kapsar.Usp Labs isterse icinde 1.3 olan urunler uretip dunyanin geri kalaninda satabilir fakat aci gercek, bu tur urunlerde ana pazar ABD'dir ve abd temelli firmalar,FDA'nin agzine bakar, oyle karar verir.1.3 satisi yasaklanmadi.Abd sinirlari dahilinde, icinde 1.3 olan supp'larin satisi yasaklandi.Zaten forumlarda salla abi ayrica toz olarak alir katariz diyor millet.Usp labs ve bb'ye mail atacagim yarin.Cevabi yazarim.
Son düzenleme:
- Durum