US SB1310 | 2011-2012 | 112th Congress
Status
Spectrum: Partisan Bill (Democrat 2-0)
Status: Introduced on June 30 2011 - 25% progression, died in committee
Action: 2011-06-30 - Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S4294-4295)
Pending: Senate Health, Education, Labor, And Pensions Committee
Text: Latest bill text (Introduced) [PDF]
Status: Introduced on June 30 2011 - 25% progression, died in committee
Action: 2011-06-30 - Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S4294-4295)
Pending: Senate Health, Education, Labor, And Pensions Committee
Text: Latest bill text (Introduced) [PDF]
Summary
Dietary Supplement Labeling Act of 2011 - Amends the Federal Food, Drug, and Cosmetic Act (FFDCA) to expand the registration requirements for a dietary supplement manufacturing facility to: (1) require the submission of a description, ingredient list, and label and labeling for each dietary supplement product manufactured; and (2) require a manufacturer to update its registration for new, reformulated, or discontinued products within 30 days. Requires the Secretary of Health and Human Services (HHS) to compile a list of dietary supplement ingredients and proprietary blends of ingredients that the Secretary determines could cause potentially serious adverse events, drug interactions, contraindications, or potential risks to subgroups such as children and pregnant or breastfeeding women. Directs the Secretary to enter into a contract with the Institute of Medicine to: (1) evaluate the safety of dietary supplement ingredients and proprietary blends of ingredients that the Institute determines could cause potentially serious adverse events, drug interactions, contraindications, or potential risks to subgroups; and (2) identify proprietary blends of ingredients for which the weight per serving of the ingredient in the proprietary blend should be provided on the label. Deems a dietary supplement that does not meet the requirements of this Act to be misbranded. Requires the Secretary to establish a definition for the term “conventional food” for purposes of the FFDCA, taking in account foods marketed as dietary supplements.
Title
Dietary Supplement Labeling Act of 2011
Sponsors
Sen. Richard Durbin [D-IL] | Sen. Richard Blumenthal [D-CT] |
History
Date | Chamber | Action |
---|---|---|
2011-06-30 | Senate | Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S4294-4295) |
Subjects
Administrative law and regulatory procedures
Agriculture and food
Child health
Department of Health and Human Services
Food industry and services
Food supply, safety, and labeling
Licensing and registrations
Marketing and advertising
Nutrition and diet
Women's health
Agriculture and food
Child health
Department of Health and Human Services
Food industry and services
Food supply, safety, and labeling
Licensing and registrations
Marketing and advertising
Nutrition and diet
Women's health
US Congress State Sources
Type | Source |
---|---|
Summary | https://www.congress.gov/bill/112th-congress/senate-bill/1310/all-info |
Text | https://www.congress.gov/112/bills/s1310/BILLS-112s1310is.pdf |