Submissions may address the statement and/or the target date for implementation.
Please complete the Medsafe consultation submission form: Sedating antihistamines label statements consultation submission form (Adobe pdf document, 3 pages, 52 KB) Sedating antihistamines label statements consultation submission form (Microsoft Word document, 3 pages 34 KB) Submissions must include full personal or organisational contact details (including address, telephone number or email address).
If you do not wish to be identified with your submission, or if you do not wish your submission to be associated with a party, you must specifically request this in the space provided on the submission coversheet.
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Read more The main reason behind the variability of effects that each type of Kratom Strain and Vein colour depicts uniquely is because of the change in the balance of the Kratom Alkaloids. Read more Host of America’s Lawyer Mike Papantonio joins RT America’s Ed Schulz and explains how big pharmaceutical companies are pushing the FDA to criminalize kratom. Read more The US Food and Drug Administration (FDA) has sent out warning letters to three US companies for illegally selling “unapproved” kratom products, that had claims that the product can treat opioid...
Read more Three companies involved in kratom supplements have received warnings from the U. Food and Drug Administration for illegally selling unapproved drug products containing kratom, not to mention...
Minutes of the 58th MCC meeting Document released for consultation on 2 August 2017.
Interested parties should respond by close of business 29 September 2017.
In addition, a list of parties making submissions may be published.
These reasons must meet Official Information Act 1982 requirements if the submission (or part thereof) is not to be displayed.
The Official Information Act criteria is available here.
“Officials say what’s in the drug is still a mystery” How is this possible.
Kratom, Mitragyna speciosa has been studied intensively all...