The Food and Drug Administration (FDA) in Manila issued an advisory on July 06 against herbal products having no labels.
Ang FDA ay nakatanggap ng mga salaysay o reklamo ukol sa paggamit ng mga PRODUKTONG HERBAL NA WALANG LABEL na nagdulot ng masamang epekto sa tao. Ang publiko ay pinaaalalahanan na mag-ingat at huwag uninom o gumamit ng mga produktong ito (FDA has received complaints regarding unlabeled herbal products. Everyone is reminded to be wary and not to take these products)," according to Advisory 2010-007 signed by FDA Director Nazarita Tacandong.
Further, the advisory warns the public that products not registered with FDA may have no proof of safety or scientific basis of therapeutic effect. "Hindi rehistrado sa FDA ang mga produktong herbal na ito kung kaya walang siyentipikong pagsasaliksik at dokumentadong mga patunay na ligtas at epektibo ang paggamit nito".
This comes a month since FDA in Manila has given full support to Administrative Order 2010-0008 of the Department of Health (DOH), which informed the public that food/dietary supplements are not drugs and should not be used to treat disease.
In requiring manufacturers to translate "No Approved Therapeutic Claims" into Filipino in herbal product labels, the herbal industry through CHIPI (Chamber of Industries of the Philippines, Inc) immediately filed a petition before the Manila Regional Trial Court. Judge Lucia Purugganan then issued a preliminary injunction order to temporarily stop the DOH directive and maintain the status quo until the issue will have been resolved by the two parties.
Read DOH-FDA Advisory 2010-007
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