S.Amdt. 1849Senate109th Congress (2005-2007)2nd degree

To express the sense of Congress with respect to over-the-counter sunscreen.

What it does: Rewrites the text S.Amdt. 1818 would insert
Submitted September 21, 2005

What it changes

1 change to S.Amdt. 1818 · shown in S.Amdt. 1818's text

Rewrites the amendment
  1. Rewrites the text S.Amdt. 1818 would insert

    Rewrites S.Amdt. 1818In place of the text S.Amdt. 1818 would insert

    In S.Amdt. 1818 as proposed

    Sec. 7[struck: ][inserted: ___]. (a) Congress makes the following findings:

    (1) Consumers need clear and consistent information about the risks associated with exposure to the sun, and the protection offered by over-the-counter sunscreen products.

    (2) The Food and Drug Administration (referred to in this section as the "FDA") began developing a monograph for over-the-counter sunscreen products in 1978.

    4 unchanged paragraphs

    (3) In 2002, after 23 years, the FDA issued the final monograph for such sunscreen products.

    (4) One of the most critical aspects of sunscreen is how to measure protection against UVA rays, which cause skin cancer.

    (5) The final sunscreen monograph failed to address this critical aspect and, accordingly, the monograph was stayed shortly after being issued until issuance of a comprehensive monograph.

    (6) Skin cancer rates continue to rise, especially in younger adults and women.

    (7) Pursuant to section 751 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 379r), a Federal rule on sunscreen labeling would preempt any related State labeling requirements.

    (8) The absence of a Federal rule could lead to a patchwork of State labeling requirements that would be confusing to consumers and unnecessarily burdensome to manufacturers.

    (b) [struck: Not ][inserted: It is the sense of Congress that the FDA should, not ]later than one year after the date of enactment of this Act, [struck: the FDA shall ]issue a comprehensive final monograph for over-the-counter sunscreen products, [struck: which shall include ][inserted: including ]UVA and UVB labeling requirements[inserted: , in order to provide consumers with all the necessary information regarding the dangers of skin cancer and the importance of wearing sunscreen].

    Original wording

    In lieu of the matter proposed to be inserted, insert the following:

Read automatically from the Congressional Record. Check the original before relying on it.

As printed

SA 1849. Mr. KOHL (for Mr. Dodd) proposed an amendment to amendment SA 1818 submitted by Mr. Dodd (for himself, Mr. Harkin, Mr. Reed, Mr. Carper, Mr. Biden, and Mr. Lieberman) to the bill H.R. 2744, making appropriations for Agriculture, Rural Development, Food and Drug Administration, and Related Agencies for the fiscal year ending September 30, 2006, and for other purposes; as follows:

In lieu of the matter proposed to be inserted, insert the following:

Sec. 7___. (a) Congress makes the following findings:

(1) Consumers need clear and consistent information about the risks associated with exposure to the sun, and the protection offered by over-the-counter sunscreen products.

(2) The Food and Drug Administration (referred to in this section as the “FDA”) began developing a monograph for over-the-counter sunscreen products in 1978.

(3) In 2002, after 23 years, the FDA issued the final monograph for such sunscreen products.

(4) One of the most critical aspects of sunscreen is how to measure protection against UVA rays, which cause skin cancer.

(5) The final sunscreen monograph failed to address this critical aspect and, accordingly, the monograph was stayed shortly after being issued until issuance of a comprehensive monograph.

(6) Skin cancer rates continue to rise, especially in younger adults and women.

(7) Pursuant to section 751 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 379r), a Federal rule on sunscreen labeling would preempt any related State labeling requirements.

(8) The absence of a Federal rule could lead to a patchwork of State labeling requirements that would be confusing to consumers and unnecessarily burdensome to manufacturers.

(b) It is the sense of Congress that the FDA should, not later than one year after the date of enactment of this Act, issue a comprehensive final monograph for over-the-counter sunscreen products, including UVA and UVB labeling requirements, in order to provide consumers with all the necessary information regarding the dangers of skin cancer and the importance of wearing sunscreen.

Legislative Activity

Stay on top of the latest movement without scrolling through every action

4 earlier actions
Floor Latest Action

Senate amendment submitted

September 21, 2005

View full timeline
Floor

Senate amendment submitted

September 21, 2005

Floor

Senate amendment proposed (on the floor): Amendment SA 1849 proposed by Senator Kohl for Senator Dodd to Amendment SA 1818.(consideration: CR S10286-10287; text: CR S10286)

September 21, 2005

Floor

Senate amendment agreed to: Amendment SA 1849 agreed to in Senate by Voice Vote.

September 21, 2005

Floor

Amendment SA 1849 proposed by Senator Kohl for Senator Dodd to Amendment SA 1818. (consideration: CR S10286-10287; text: CR S10286) To express the sense of Congress with respect to over-the-counter sunscreen.

September 21, 2005

Floor

Amendment SA 1849 agreed to in Senate by Voice Vote.

September 21, 2005