I-FDA ngenkuthalo "ibeka iliso kwi-intanethi ye-ecosystem yeemveliso zobuqhetseba ezithengiswa ngabadlali ababi abafuna ukwenza inzuzo kulo bhubhani wehlabathi."Le arhente ithi ifumene amakhulukhulu eemveliso zobuqhetseba ze-COVID-19, kubandakanya iziyobisi, izixhobo zovavanyo, kunye nePPE ezithengiswa kwi-Intanethi ngamabango angangqinwanga.Isebenza kunye neemarike ze-intanethi, iirejistra zegama lesizinda, iiprosesa zentlawulo, kunye newebhusayithi yeendaba zentlalo ukususa amabango angabonakaliyo kumaqonga abo.

Ukuza kuthi ga ngoku, i-FDA ikhuphe ngaphezulu kweeleta ezingama-65 ezilumkisayo.Kwiimeko ezithile, i-FDA ilandele ezo leta zesilumkiso ngokucela i-DOJ ukuba iqalise iinkqubo zomthetho ezisesikweni ngokuchasene nomvelisi wemveliso.Kwezinye iindidi zeemveliso, i-FDA isebenzise izibhengezo zeendaba ukubonelela ngokufanelekileyo isilumkiso esiqhelekileyo kubo bonke abavelisi abakwisithuba.Apha ngezantsi sidwelisa zonke iinzame zokunyanzeliswa ebezisetyenziswa yi-FDA ukuzama ukugcina iimveliso ezinobuqhophololo ze-COVID-19 zingekho emarikeni.

I-FDA kunye ne-FTC bathumele umjikelo wabo wokuqala weeleta ezilumkisayo kwiinyanga ezintathu ezidlulileyo.Ngoku, i-FDA ikhuphe ubuncinci iileta ezilumkisayo ezingama-66 kwiifemu ezithengisa iimveliso ezinobuqhophololo ngamabango okuthintela, ukuxilonga, ukunyanga, ukunciphisa, okanye ukunyanga i-COVID-19.

Iimveliso ziquka (1) iimveliso ze-CBD, (2) izongezo zokutya kunye neevithamini, (3) i-oyile ezibalulekileyo, (4) iimveliso zemifuno, (5) iimveliso ze-homeopathic, (6) iimveliso ze-sanitizer, (7) iimveliso ezibhalwe ukuba zine-chlorine dioxide. okanye isilivere ye-colloidal, kunye (8) nabanye.I-FDA ithathele ingqalelo amabango ahlukeneyo okuthengisa-ukususela kwi-#coronavirus hashtag ukuya kwiingxelo ezenziwe kwiifestile ezizivelelayo.Itshathi engezantsi idwelisa iileta zezilumkiso ngokodidi lwemveliso kwaye ichonge ezinye zeengxelo eziyingxaki ezichongwe yi-FDA.Le tshathi yereferensi kufuneka ibe luncedo ekuboneni ukuba i-FDA igxile phi kwiinzame zayo zokunyanzelisa xa isiza kumabango e-COVID-19.Uqhagamshelwano oluya kwiileta ezilumkisayo lukwabonelelwe ngemveliso nganye.

Iprotokholi yeCoronavirus (iTea yeBoneset yeCoronavirus, ukuKhuselwa kweSeli yeCoronavirus, i-Coronavirus Core tincture, iNkqubo yokuKhusela i-Coronavirus, kunye ne-Elderberry Tincture)

“Quicksilver Liposomal Vitamin C w/ Liposomal,” “Jigsaw Magnesium With SRT,” kunye neemveliso ezibhalwe ukuba zinesilivere

"I-Superblue Silver Immune Gargle," "Intlama yamazinyo emhlophe eSuperSilver," "Ijeli yokunxiba yamanxeba eSuperSilver" kunye "nentlama yamazinyo yasimahla yeFluoride"

I-HealthMax Nano-Silver Liquid, iiSilver Biotics zeSilver Lozenges ezineVithamin C, kunye neSilver Biotics yeSiliva yeGel Ultimate yoLusu kunye noNyango loMzimba (ngokudibeneyo, "iimveliso zakho zesilivere")

Isilivere, iimveliso ze-CBD, i-iodine, i-mushroom yamayeza, i-selenium, i-zinc, i-vitamin C, i-vitamin D3, i-astragalus, kunye ne-elderberry.

"I-China Oral Nosode," ichazwa njenge "AN330 - INKXASO YOMZIMBA WE-CORONA KUNYE / OKANYE UKOsuleleka OLUSEBENZAYO LOKUPHILA KUYO YONKE Iminyaka"

Iileta zesilumkiso ze-FDA ziye zanda zaya kumanyathelo asemthethweni ubuncinane kwiimeko ezimbini.Njengoko besixele ngaphambili, i-FDA ilumkise umthengisi weemveliso ze-chlorine dioksidi ukuba asuse iimveliso zayo kwintengiso kwiiyure ezingama-48.Emva kokuba umthengisi "ecacisile ukuba akananjongo yokuthatha amanyathelo okulungisa," i-DOJ yafumana umyalelo wokuthintela okwethutyana ngokuchasene nayo.

Ngokukwanjalo, i-DOJ yafumana umyalelo wokuthintelwa okwexeshana kumthengisi weemveliso zesilivere ezididiyelwe owathi, nangona “esusa [e]susa amaphepha ewebhu anxulumene ne-COVID-19 okwexeshana, ...baphinde baqala ukuthengisa iimveliso zabo zesilivere ye-colloidal njengonyango lwe-COVID-19 ngokuchasene nomthetho. "

Kuzo zombini ezi meko, i-FDA ibonise ukunqongophala kwedatha eyaneleyo yokuseka ukhuseleko kunye nokusebenza kweemveliso zayo "nakuphi na ukusetyenziswa," singasathethi ke ngenoveli coronavirus.Le arhente ivakalise inkxalabo yokuba amabango anjalo anokubangela ukuba abathengi balibazise okanye bayeke unyango olufanelekileyo.Nangona yanika abavelisi bemveliso ithuba lokuthatha amanyathelo okulungisa, ekugqibeleni yalandela isoyikiso lokuthatha amanyathelo asemthethweni.

I-FDA ikwasebenzise izibhengezo zemihla ngemihla ukunxibelelana nabavelisi beemveliso ze-COVID-19, ngakumbi uvavanyo lwasekhaya kunye nabavelisi be-serology.

Kwesinye isibhengezo, i-FDA yalumkisa ukuba ayigunyaziswanga naluphi na uvavanyo lokuziqokelela-ngaphandle kovavanyo olwalulungiselela ukubetha imarike.Kutshanje ibonise ukuvuleleka ngakumbi kumbono, nangona kunjalo.Njengoko besixele ngaphambili, inike ugunyaziso losetyenziso olungxamisekileyo (EUA) kwikiti yokuqokelela ekhaya, ikiti yokuqokelela amathe esekwe ekhaya, kunye nekiti yokuqokelela ezimele ekhaya.Sele iqalile ukubonelela ngeSifanekiso seKhaya lokuQokelelwa kweMolekyuli yoDiagnostic EUA ukuxhasa ngakumbi uphuhliso lovavanyo lokuziqokelela ekhaya.

Ngokufanayo, i-FDA ipapashe izibhengezo ezininzi zeendaba ezifana nale ichaza ukuma kwayo kuvavanyo lwe-serology.I-arhente ngaphambili igcine umgaqo-nkqubo ophumle ngokufanelekileyo wovavanyo lwe-serology, ukusukela phakathi kuMatshi, ivumela iimvavanyo ze-antibody zorhwebo ukuba zithengiswe kwaye zisetyenziswe ngaphandle kokuphononongwa kwe-FDA EUA ukuba balandela iindlela ezithile.Kodwa i-FDA ihlaziye lo mgaqo-nkqubo kwinyanga ephelileyo, kwakamsinya nje emva kokuba ikomitana yenkongolo yagxeka le arhente “ngokungaphumeleli [kungamapolisa]” imakethi yovavanyo lwe-coronavirus serological antibody.

INKCAZELO: Ngenxa yokuqheleka kolu hlaziyo, ulwazi olunikwe apha alunakusetyenziswa kuzo zonke iimeko kwaye akufuneki luthathwe ngaphandle kweengcebiso ezithile zomthetho ezisekelwe kwiimeko ezithile.

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