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» Revised Effectiveness Determination; Sunscreen Drug Products for Over-the-Counter Human Use
Revised Effectiveness Determination; Sunscreen Drug Products for Over-the-Counter Human Use
Document ID:
FDA-1978-N-0018-0699
Document Type:
Proposed Rule
Agency:
Food And Drug Administration
Topics:
Drugs, Labeling, Reporting and Recordkeeping Requirements
Federal Register Number:
2011-14769
CFR Citation:
21 CFR Part 201
View Document:
Details Information
Document Subtype:
Notice of Proposed Rulemaking (NPRM)
Received Date:
June 17 2011, at 12:00 AM Eastern Daylight Time
Start-End Page:
35672 - 35678
Page Count:
7
Comment Start Date:
June 17 2011, at 12:00 AM Eastern Standard Time
Comment Due Date:
September 15 2011, at 11:59 PM Eastern Standard Time
Comments
View All
Total:
13
Yakeema S. Mercer - Comment
Posted:
09/21/2011
ID:
FDA-1978-N-0018-0708
Comment Period Closed
Sep 15,2011 11:59 PM ET
Brett Glass - Comment
Posted:
09/21/2011
ID:
FDA-1978-N-0018-0709
Comment Period Closed
Sep 15,2011 11:59 PM ET
American Academy of Dermatology (AAD) Association - Comment
Posted:
09/21/2011
ID:
FDA-1978-N-0018-0710
Comment Period Closed
Sep 15,2011 11:59 PM ET
Consumers Union (CU) - Comment
Posted:
09/21/2011
ID:
FDA-1978-N-0018-0712
Comment Period Closed
Sep 15,2011 11:59 PM ET
Johnson & Johnson Consumer & Personal Products Worldwide - Comment
Posted:
09/21/2011
ID:
FDA-1978-N-0018-0713
Comment Period Closed
Sep 15,2011 11:59 PM ET
Related Documents
Total:
3
Labeling and Effectiveness Testing: Sunscreen Drug Products for Over-the-Counter Human Use - Notice of Correction
Requests for Exemption From the Bar Code Label Requirements; Change of Address
Final Monograph: Organ-Specific Warnings; Internal Analgesic, Antipyretic, and Antirheumatic Drug Products for Over-the-Counter Human Use
Revised Effectiveness Determination; Sunscreen Drug Products for Over-the-Counter Human Use
Details Information
Comments
View AllPosted: 09/21/2011 ID: FDA-1978-N-0018-0708
Sep 15,2011 11:59 PM ET
Posted: 09/21/2011 ID: FDA-1978-N-0018-0709
Sep 15,2011 11:59 PM ET
Posted: 09/21/2011 ID: FDA-1978-N-0018-0710
Sep 15,2011 11:59 PM ET
Posted: 09/21/2011 ID: FDA-1978-N-0018-0712
Sep 15,2011 11:59 PM ET
Posted: 09/21/2011 ID: FDA-1978-N-0018-0713
Sep 15,2011 11:59 PM ET
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