HBW Insight is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

Astringent rule

This article was originally published in The Rose Sheet

Executive Summary

Effective date for direct final rule for astringents marketed under the OTC Skin Protectant Monograph is June 13, 2004, FDA says in a Jan. 22 Federal Register notice correcting an earlier published effective date of Oct. 27, 2003. FDA published an amended final rule for skin protectant astringent drug products in June and included small packaging exemptions and minor labeling changes along with the incorrect effective date (1"The Rose Sheet" June 16, 2003, p. 10)...

You may also be interested in...



Astringent Final Rule Contains Revised Labeling, Small Package Exemptions

The Skin Protectant Astringent direct final rule includes minor labeling changes and small packaging exemptions to bring the astringent portion of the Skin Protectant Monograph in line with the rest of the rule, FDA says. The agency published the direct final rule in the Federal Register June 13

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.

Latest Headlines
See All
UsernamePublicRestriction

Register

RS011834

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel