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2010-09-24
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Medical Devices; Labeling for Menstrual Tampons; Ranges of Absorbency
Proposed Rules
D09002ee1bdfe2d49
D09002ee1bdfe2dc4
United States
Department of Health and Human Services
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United States Government Agency or Subagency
United States
Food and Drug Administration
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United States Government Agency or Subagency
The Food and Drug Administration (FDA) is proposing to amend its menstrual tampon labeling regulation to provide an absorbency term for tampons that absorb 15 to 18 grams (g) of fluid. The purpose of this proposed rule is to enable consumers to compare the absorbency of one brand and style of tampons with the absorbency of other brands and styles. FDA is issuing this proposed rule under the Federal Food, Drug, and Cosmetic Act (the act).
64 FR 3255
https://www.govinfo.gov/app/details/FR-1999-01-21/99-1362
99-1362
fr21ja99-18
4160-01-F
Docket No. 98N-0970
https://www.govinfo.gov/app/details/FR-1999-01-21/99-1362
https://www.govinfo.gov/content/pkg/FR-1999-01-21/html/99-1362.htm
https://www.govinfo.gov/content/pkg/FR-1999-01-21/pdf/99-1362.pdf
3 p.
3255
3257
64 FR 3255
Code of Federal Regulations
Title 21 Part 801
21 CFR Part 801
Medical Devices; Labeling for Menstrual Tampons; Ranges of Absorbency; Federal Register Vol. 64, Issue
PRORULE
99-1362
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
1999-04-21
Docket No. 98N-0970
4160-01-F
99-1362
Proposed rule.
The Food and Drug Administration (FDA) is proposing to amend its menstrual tampon labeling regulation to provide an absorbency term for tampons that absorb 15 to 18 grams (g) of fluid. The purpose of this proposed rule is to enable consumers to compare the absorbency of one brand and style of tampons with the absorbency of other brands and styles. FDA is issuing this proposed rule under the Federal Food, Drug, and Cosmetic Act (the act).
Written comments on the proposed rule should be submitted by April 21, 1999. See section II of this document for the proposed effective date of a final rule based on this document. Written comments on the information collection requirements should be submitted by February 22, 1999.
Colin M. Pollard, Center for Devices and Radiological Health (HFZ-470), Food and Drug Administration, 9200 Corporate Blvd., Rockville, MD 20850, 301-594-1180.
Federal Register
Vol. 64, no. 13
Office of the Federal Register, National Archives and Records Administration
1999-01-21
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202 p.
Table of Contents:
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GS 4.107:
AE 2.106:
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https://www.govinfo.gov/app/details/FR-1999-01-21
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0042-1219
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000582072
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https://www.govinfo.gov/app/details/FR-1999-01-21
https://www.govinfo.gov/content/pkg/FR-1999-01-21/pdf/FR-1999-01-21.pdf
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FR-1999-01-21
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