Claritin label change
This article was originally published in The Tan Sheet
Executive Summary
FDA approves Schering-Plough's request to add the descriptor "Indoor & Outdoor Allergies" to the principal display panel of 10- and 30-count carton labels of Claritin Liqui-Gels (loratadine 10 mg), according to an April 6 letter. The change could extend the medicine's benefits beyond seasonal allergies. FDA approved a similar change to Claritin packaging in 2008 (1"The Tan Sheet" Jan. 28, 2008, In Brief)
You may also be interested in...
FDA approves new Claritin label
FDA will allow Schering-Plough to communicate on its product label that Claritin relieves both indoor and outdoor allergies, potentially extending the OTC non-drowsy allergy medicine's benefits beyond seasonal allergy treatment. Previously, labels could only state that Claritin relieves outdoor allergies, S-P says Jan. 22...
US Q1 Consumer Health Earnings Preview: Label This One Historic And Challenging But Promising
US OTC drug and supplement firms’ reports of results for the first three months of 2024 began on April 19 with P&G. JP Morgan analysts say while “some retailers in the US in particular” are reducing consumer health inventories, for the overall sector they expect “a healthier balance of positive volume and lower pricing contribution.”
Keeping Track: Cancer Approvals From Lumisight Imaging To Adjuvant Alecensa
The US FDA’s approval of Lumicell’s optical imaging agent Lumisight makes a dozen novel approvals in 2024 for the Center for Drug Evaluation and Research.