Regulators are taking a closer look after finding asbestos, a known
carcinogen, in several talc cosmetics and powders, including a
bottle of Johnson & Johnson’s well-known Baby Powder. Citing those
FDA results, some U.S. lawmakers and consumer advocates have called
for stricter safety regulations to protect public health.
J&J, the market leader in talc powders, has defended the safety of
its talc. The company said tests by labs it hired found no asbestos
in samples from the same bottle the FDA examined - except for some
the company attributed to contamination from a lab air conditioner.
In a statement, the company said it looks forward to the FDA’s
"thorough review of the most effective and reliable ways to test for
asbestos in cosmetic talc."
The hearing on asbestos testing in talc, the FDA’s first since 1971,
will focus on testing standards recommended by a panel of government
experts. The recommendations, published last month, embrace
positions held by public health authorities and experts for
plaintiffs who allege that contaminated talc products caused their
cancers.
After hearing from the government panel, FDA officials will take
public comment from consumer advocates, industry representatives and
testing experts.
For decades, the cosmetic talc industry has largely been allowed to
police itself with little oversight from the FDA. Although talc and
asbestos are similar minerals often found together in the ground,
the FDA has never required manufacturers to test for the carcinogen.
In a written report, the government panel said the talc industry’s
standard test methods have "long-recognized shortcomings in
specificity and sensitivity."
One of the most significant recommendations from the expert panel is
that mineral particles found in talc products small enough to be
drawn into the lungs, even those the industry would not call
asbestos, should be counted as potentially harmful. The expert panel
said both asbestos and look-alike minerals are suspected of causing
"similar pathological outcomes," so the "distinction is irrelevant."
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The U.S. Occupational Health and Safety Administration and the
Environmental Protection Agency have limited exposure to asbestos on
the job and in the air to reduce cancers since the 1970s when the
hazard was well established. A Reuters report in December (https://www.reuters.com/
investigates/special-report/usa-health-fda-talc) showed that, during
the same period, the FDA downplayed health concerns, including
possible asbestos contamination, in talc powders and cosmetics and
deferred again and again to manufacturers.
David Michaels, a former OSHA administrator during the Barack Obama
administration, said he welcomed the public discussion because even
small amounts of asbestos are unacceptable in easily-inhaled
consumer products.
"I hope the national attention given to this issue will help
insulate FDA from pressure from corporations that manufacture
cosmetics and personal care products, who are likely to oppose the
newly-recommended testing protocols," said Michaels, a professor at
the George Washington University School of Public Health and author
of a book, "The Triumph of Doubt," which examines corporate
influence on science.
The Personal Care Products Council, a cosmetics trade group,
declined to comment before the hearing.
FDA spokeswoman Monique Richards said no decisions are expected to
be made Tuesday, and the focus will be on gathering public feedback.
The FDA has not announced a timetable for deciding whether it will
pursue rules on testing.
The increased scrutiny on this issue follows a 2018 Reuters report
(https://www.reuters.com/
investigates/special-report/johnsonandjohnson-cancer) which showed
that although J&J knew for decades its raw talc and powders
sometimes tested positive for asbestos, the company did not report
those findings to the FDA.
(Reporting by Chad Terhune)
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