Document aJZ15z4XVZqZEZQ7bazxqq40Y
Mr. Anthony Romero Criteria Manager Division of Criteria Documentation
& Standards Development NIOSH - BA-37 5600 Fishers Lane Rockville, Maryland 20852
Dear Mr. Romero:
'
The Cosmetic, Toiletry and Fragrance Association, Znc. (CTFA)
is a national trade association representing the cosmetic
industry. Zt includes more than two hundred active member
companies which manufacture or distribute finished cosmetic
products in the United States. Zn addition, CTFA includes
more than two hundred Associate member companies from related
industries, such as manufacturers of cosmetic raw materials
and packaging materials. Ve estimate the CTFA members are
responsible for more than 90% of the cosmetic products manu
factured and distributed in the United 8tates.
The CTFA Talc Subcommittee read with concern the first and second drafts of the Stanford Research Institute report to KIOSE entitled, "TALC''. This Subcommittee, which is composed of industry scientists from various disciplines including mineralogy, offers the following comments which we hope will be helpful in the preparation of subsequent drafts: I. CTFA STANDARD FOR COSMETIC GRADE TALC
The Stanford Research Institute, in developing this Talc Document, has opted not to provide recognition to the
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PLAINTIFFS EXHIBIT
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voluntary purity standard (Attachment 1) established in October, 1976 by the CTFA lor Cosmetic Talcs. ^ 2 ^ Cosmetic Grade Talcs, which specify a composition of 90% hydrated magnesium silicate and the absence of detectable asbestos, should not be grouped with industrial talcs of lower and less defined purity in the development of occu pational hygiene standards.
Unlike that of very impure talc mixtures, the pathogenicity of high purity talcs (conforming to the CTFA Standard) has been extensively and carefully evaluated (References 1-10). It is stressed that these carefully defined studies must be distinguished from historic literature citations1 loose generic reference^to the term 'cosmetic talc'^tyhich only denote physical and tactile properties deemed appropriate for cosmetic use, but carried no universal meaning in terms of mineral composition or contaminants.
An extensive CTFA presentation has been made to the FDA/OTC i
Antipersplrant Drug Review Panel in July, 1975 in support of -tie CpP^A Cosmetic Grade TalcX as a safe and useful ingredient (Attachment 3). Similar positive reviews of data were conducted by the FDA/OTC Miscellaneous External Drug Review Panel in August, 1977 and the FDA/OTC Anti microbial II Drug Review Panel in January, 1977. Other reviewers (Attachments A,5,6,7,8) have also concluded that CTFA cosmetic talcs are not hazardous to its users.
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There have been old reports in the literature of unsub stantiated findings of chrysotile asbestos in talcs. However, these mistakened detections of chrysotile were actually chlorite mineral, mis-identified in X-ray Dif fraction through negligent confirmatory analyses. In your review of the CTFA Cosmetic Talc Standard^ you will note the absence of a specification for chrysotile. This was supported and dictated by the absence of chrysotile. verified through a round robin study of 3,397 samples of cosmetic talcs from sources such as Montana, Vermont, Alabama, North Carolina and Italy. The results of this round robin study were submitted to the Food and Drug Administration in September, 1975 (Attachment 2).
II. BASIS FOR TLV AMENDMENT
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There is no firm basis for projecting and amending the
permissible occupational exposure limit. The available
research data cited in the S.R.I. report suffer from a
common deficiency of Incomplete dust analysis and exposure
measurements during the entire period of workers' exposure.
The S.R.I. March 1970 report itself stated that tt)e data
available are insufficient to draw valid conclusions.
For example:
- lines 5098, 5099 and 5100
"More comprehensive epidemiologic studies concerning exposure to talc without asbestos minerals are needed with follow-up studies of populations and cohorts
' already reported on." .
- lines 5141, 5142 and 5144
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"Animal inhalation studies that evaluate the
degrees of pathogenic effects on pulmonary
tissue of pure talc, dolomite, chlorite, magnesite,
non-flbrous tremollte,' and th talc-related
mineral pyrophyllite, alone and in combination,
are needed."
.
- lines 4041, 4042 and 4043
..
"...the evidence presented in any one ol these papers (17, 65, 68) is not conclusive for the purposes of setting a permissible exposure limit...
Various intimately-informed reviewers In the NIOSH Experts,
Government Agency and External Panel have also commented
on the inadequacies of the epidemiologic studies, for
example:
Burgess, V.A. - External Reviewer A.l.H.A.
"....many of the early studies Involved exposures to >10 mg/m3 to a talc containing concentrations of free silica up to 18%."
"....It was not possible to obtain historical data for the previous decade. It is possible that a range of talcs were in use and the concentrations were higher than those noted during the environmental component of this study."
"The Selevan study does not present exposure data..."
Peters, J.H. - NIOSH Expert Reviewer
...Rubino's study adds little useful information to standard setting."
"Selevan1s study contains little reliable environmental information to match up with the health effects."
Thiessen, J.V. - Agency Reviewer, Dept, of the Army
"From an epidemiological perspective....none of the articles or studies cited establishes a direct causal relationship between non-asbestlform talc containing less than 1% quartz and a disease state."
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"None of the evidence given demonstrates a reasonable model that shows the'old standard as being too high."
"More toxicological data is needed concerning the health elfeets of relatively pure talc and talc with Its associated minerals....as well as epidemiologic studies on occupationally exposed persons. Establishment of a new standard should be contingent on such studies."
Damstraj T. - Agency Reviewer, NIEH5
#
"Many of the studies cited did not adequately characterize talc by mineral composition, particle size, or purity...."
Uarkle, R.A. - Agency Reviewer, Bureau of Mines
"The exhaustive 87 page section on biological effects of exposure describes mainly studies done at concen trations much greater than the current TLV of approximately 3.0 milligrams per cubic meter or where the talc contained silica or asbestos."
CTFA agrees with S.R.I. that "the evidence presented by
the literature references is not conclusive for the
purpose of setting a permissible exposure." Ve also
agree with S.R.I. that further epidemiological studies
should be carried'out, but urge that these should be
designed toward projecting a recommended permissible
exposure level which is based on determined exposures to
talc that has been properly analyzed and shown to be in
the category to be regulated. Until more valid data are
generated, a lowering of the present TLV for CTFA Cosmetic
Talc is wholly arbitrary and an unwarranted inflationary
action.
III. LABELING AND POSTING
J*
In the prevailing absence of direct occupational eause
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and effect data, the proposed label and posting warnings which specifically single out Talc are unjustified and prejudicial., This type of warning language wrongly implies to the worker and the public that a high purity talc such as " C ^ A Cosmetic Grade Talc" is very toxic. The CTFA would endorse the recommendation for training and counseling under Section 5, page 9 as an effective documentable and controllable awareness tool in the handling of any general dust substance. However, we find the labeling and posting requirement to be a redundant, passive means of employee communication. If NIOSH still considers warnings and postings to be necessary, then they should reflect the uncertainty of the data supporting this need. Therefore, it would be more appropriate to UBe language such as:
DUST EXCESSIVE INHALATION HAT CAUSE
ADVERSE RESPIRATORY EFFECTS MEDICAL In view of the known adverse effects of x-ray radiation, it is recommended that the medical surveillance require ments specify that a frontal view be done, followed by a side view only When necessary.
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V. WORE PRACTICES We recommend that NXOSH follow OSHA's recent standard setting precedence of stipulating performance type standards. It is preferable that examples of acceptable controls and work practices be provided as appendices and not as standards. In this manner OSHA would not Inhibit Innovative control techniques.
VI. ACTION LEVEL The "action level" of the SRI document serves no purpose. We understand an "action l e v e l t h a t level above which medical, labeling and posting, personnel protective equip ment, training, monitoring and record keeping take effect.
According to lines 52 to 58:
.
"The "action level" is defined as a concentration in the air of the workplace at or above one-half the recommended environmental limit (see Section 1). Exposure to talc at LOWER concentrations requires adherence to the following sections 2, 3 (a and b), 4, 5, 6, 7 and 8 (a and c)."
The work LOWER inplies that any measurable level down to_
zero activates the standard requirement as an "action
level." We find this contrary to all existing OSHA standards
and directives and indeed more stringent than any other
standard, including the asbestos standards. This amounts
to promulgating a aero standard.
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The CTFA Talc Subcommittee hopes that the above comments
will be helpful to you, and would be pleased to provide
further assistance. In particular, the CTFA would appreciate
receiving copies of future drafts so that we may provide
additional comments and Information.
Sincerely,
Norman F. Estrin, Ph.D. Vice President~8clence
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ATTACHMENTS
S2.
Cosmetic Talc, CTFA Specification-The Cosmetic Toiletry and Fragrance Association Inc. (10/7/76 Rvision). .
Estrin, Dr. Norman, Letter to Dr. Robert Schaffner (FDA) September 23 ( 1975.
y 3 . CTFA Presentation to FDA/Over-the-Counter Antiperspirant Drug Review Panel, July 9, 1975.
y a . Hildick-Smith. G.Y., The Biology of Talc. British Journal
of Industrial Medicine 33x217-229, 1976.
y s.
Hildick-Smith, G.Y., Talc - Recent Epidemiological Studies. In Proceedings of the 4th International Symposium on Inhaled particles and Vapours. Inhaled Particles IV, Part 2: 655-'
665, Edinburgh, 1975.
./ 6 Cosmetic Talc Powder; The Lancet, No. 8026, June 25, 1977.
.y'7 Kennedy, Donald, Letter to S. M. Wolfe, B. Gordon. Public
Citizen Health Research Group, January, 1979.
/s.
GSA "Draft Commercial Item Description A-A-42 Talcum Powder",
January 16, 1979.
*
REFERENCES
I. Wehner, A.P., Zwicker, G.H., Cannon, V.C., Watson, C.R. and'Carlton, W.W.: Inhalation of Talc Baby Powder by Hamsters. Food and Cosmetics Toxicology 15:121-129, 1977.
II. Wehner, A.P., Wilkerson, C.L., Cannon, W.C., Buschbom, R.L., and Tanner, T.M.: Pulmonary Deposition, Translocation and Clearance of Inhaled Neutron-Activated Talc in Hamsters. Food and Cosmetics Toxicology 15:213-214, 1977.
III.
Wehner, A.P., Tanner, T.H., Buschbom, R.L.: Absorption of Ingested Talc by Hamsters. Food and Cosmetics Toxicology 15:453-455, 1977.
IV.'
Wilkerson, C.L., Wehner, A.P. -, and Rancitelli: Leaching of
Radionuclides from Neutron-Activated Talc in Serum and in
Dilute Hydrochloric Acid. 'Food and Cosmetics Toxicology
15:589-593, *1977.
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V. Teratologic Evaluation of EDA 71-43 (Talc), PB-221 804, Pood and Drug Research Labs., Inc., January 1973.
VI. Mutagenic Evaluation of Compound FDA 71-43, Talc. PB-245 458,
Litton Bionetics, Inc. 9 December 1974.
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VII. , Lord, G.H. : Biological Effects of Talc in the Experimental ' Animal. Food and Cosmetics Toxicology 16:51-57, 1978.
VIII. IX.
Phillips, J.C., Young, P.J., Hardy, K. and Gangolll, 8.D.: Studies on the Absorption and Disposition of SH-Labelled Talc in the Rat,' House,'Guinea-Pig and'Rabbit. Food & Cosmetics Toxicology 16:161-163 1978.
Luchtrath, H. and Schmidt, K.G., Beitr, Slllkosforsch, 61,1, 1959.
X. HacNab, G. and Harington, J.S.: Nature London, 214,522, 1967.
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