Washington State House of Representatives Office of Program Research |
BILL ANALYSIS |
Select Committee on Environmental Health | |
HB 2166
This analysis was prepared by non-partisan legislative staff for the use of legislative members in
their deliberations. This analysis is not a part of the legislation nor does it constitute a
statement of legislative intent.
Brief Description: Enacting the Washington safe cosmetics act of 2007.
Sponsors: Representatives Chase, Skinner, Hunt, O'Brien, Hudgins, Campbell, Morrell, Kirby, Hasegawa, Simpson, Haler, McCune, Kretz, Dunshee, Pettigrew, Walsh, Dickerson, Williams, Eickmeyer, Conway, Schual-Berke and Moeller.
Brief Summary of Bill |
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Hearing Date: 2/20/07
Staff: Amy McCormick (786-7290).
Background:
The federal Food, Drug, and Cosmetic Act (FD&C) and the federal Fair Packaging and Labeling
Act (FPLA) regulate cosmetics marketed in the United States. The United States Food and Drug
Administration (FDA) enforces the FD&C, which prohibits the marketing of adulterated or
misbranded cosmetics in interstate commerce. Violations of the FD&C that involve product
composition, whether resulting from ingredients, contaminants, processing, packaging, or
shipping and handling, cause cosmetics to be adulterated and subject to regulatory action.
Improperly labeled or deceptively packaged products, such as false or misleading labeling, or
incomplete label information, are considered misbranded and subject to regulatory action. In
addition, under the authority of the FPLA, the FDA requires an ingredient declaration to enable
consumers to make informed purchasing decisions. Cosmetics that fail to comply with the FPLA
are considered misbranded under the FD&C.
With the exception of color additives, cosmetic products and ingredients are not subject to FDA
pre-market approval authority. Cosmetic firms are responsible for substantiating the safety of
their products and ingredients before marketing. The Cosmetic Ingredient Review Panel is a
non-governmental body established and funded by the cosmetics industry to review the safety of
cosmetic ingredients. If a cosmetic product is not adequately substantiated, the following
warning statement must appear conspicuously on the display panel of the product's label:
"WarningThe safety of this product has not been determined." A cosmetic product that is not
adequately substantiated will be considered misbranded if this warning does not appear on the
label.
Several ingredients are prohibited or have restricted use and require warning statements on the
labels of certain types of cosmetics. In general, except for color additives and those ingredients
which are prohibited or restricted from use in cosmetics by regulation, a manufacturer may use
any ingredient in the formulation of a cosmetic provided that the ingredient and the finished
cosmetic are safe, the product is properly labeled, and the use of the ingredient does not cause the
cosmetic to be adulterated or misbranded under federal law.
The FDA may pursue enforcement action against products, firms, or individuals in violation of
the law.
The state's uniform Washington Food, Drugs and Cosmetics Act mirrors the federal FD&C in
regulating the sale in intrastate commerce of cosmetics that are adulterated or misbranded. State
law also provides injunctive relief and criminal penalties for violations. The Washington
Department of Labor and Industries (L&I) administers the Chemical Hazard Communication
rule, which requires employers to inform and train employees about hazardous chemicals in the
workplace. Retail cosmetics are exempt from this rule. The Department of Ecology (DOE)
maintains a Hazardous Substance Information and Education Office (HSIEO) that provides the
public with information about certain chemicals in the community. No state agency has authority
to identify, review, or regulate ingredients in cosmetic products that may cause chronic health
effects, unless the product is adulterated or misbranded under the Washington Food, Drugs and
Cosmetics Act.
Summary of Bill:
This bill enacts the Washington Safe Cosmetics Act of 2007.
Manufacturer Disclosure
Manufacturers of cosmetic products must provide the Department of Health (DOH) with a list of
all cosmetic products sold in the state that contain any ingredient that may cause cancer or
reproductive toxicity. Manufacturers must identify each chemical used by name and chemical
abstract service number and specify in which products the chemical is contained.
Investigation
The DOH may conduct an investigation of cosmetic products that contain chemicals identified as
causing cancer or reproductive toxicity or other ingredients of concern. An investigation may
include a review of available health effects data and studies, worksite health hazard evaluations,
epidemiological studies, and exposure assessments. The department may require manufacturers
of products subject to an investigation to submit to the department relevant health effects data
and studies available to the manufacturer, as well as other information. If the DOH's
investigation reveals that an ingredient is potentially toxic, the results of the investigation are
referred to the L&I, which then must determine whether it is necessary to develop a standard to
protect the health of employees with regular exposure to the hazard.
Enforcement
The DOH may refer any product containing an ingredient found unsafe by the Cosmetic
Ingredient Review Panel, a non-governmental body established by the cosmetics industry to
review the safety of cosmetic ingredients, to the Attorney General and the FDA for possible
enforcement under Washington law and the federal FD&C.
Penalty
Any person who violates this act is guilty of a misdemeanor.
Appropriation: None.
Fiscal Note: Preliminary available.
Effective Date: The bill takes effect 90 days after adjournment of session in which bill is passed.