WHO Pharmaceuticals Newsletter 1998, No. 11&12
(1998; 10 pages)
Table of Contents
Close this folderRegulatory actions
View the documentAcetylsalicylic acid and paracetamol: stricter controls: UK
View the documentAlcohol warning: revised labelling of all OTC pain relievers & fever reducers: USA
View the documentCamphor and/or menthol: warning concerning fire hazard: USA
View the documentCholestin: determined to be an unapproved drug: USA
View the documentCorticosteroids (inhaled and intranasal formulations): new labelling required for use in children: USA
View the documentEphedrine and atropine: not accepted in final monographs for OTC internal analgesic or menstrual use: USA
View the documentEritrityl tetranitrate: withdrawal of approval: lack of efficacy: USA
View the documentL-desoxyephedrine (levmetamfetamine): added to monograph for OTC nasal decongestant drug products: USA
View the documentMagnesium sulfate: revised labelling: UK
View the documentNucleoside analogues: revised product information: hepatic steatosis and lactic acidosis: Portugal
View the documentPovidone-iodine: warning concerning overdosage: Austria
View the documentSoy protein and coronary heart disease: new health claim proposed: USA
View the documentTick-borne encephalitis virus vaccine: paediatric formulation withdrawn: adverse reactions: Germany
Open this folder and view contentsDrug surveillance
Open this folder and view contentsNew developments
Open this folder and view contentsMedical devices
Open this folder and view contentsGeneral information
Open this folder and view contentsMedication errors
Open this folder and view contentsVeterinary medicine
 

L-desoxyephedrine (levmetamfetamine): added to monograph for OTC nasal decongestant drug products: USA

United States of America. The Food and Drug Administration has amended the final monograph for over-the-counter (OTC) nasal decongestant drug products to add the ingredient l-desoxyephedrine (levmetamfetamine) and to classify this ingredient as generally recognized as safe and effective for OTC use for the relief of nasal congestion caused by acute or chronic rhinitis. The agency is also removing the name “l-desoxyephedrine” from the list of nonmonograph active ingredients.

Reference: Federal Register 63(146): 40647-50 (1998).

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Last updated: May 3, 2013