Request for Additional Information

Attachment 4c_Request for Add Information.doc

Annual Submission of the Ingredients Added to, and the Quantity of Nicotine Contained in, Smokeless Manufactured, Imported, or Packaged in the U.S.

Request for Additional Information

OMB: 0920-0338

Document [doc]
Download: doc | pdf

«Date»


Form Approved

OMB# 0920-0338

Expiration Date: 02/28/2014

«Name»

«Company»

«Address_1»

«Address_2»

«City_State_Zip»


Dear «Salutation»:


This letter is to notify you that the Centers for Disease Control and Prevention (CDC) has begun processing the Ingredient Report recently submitted by you on «Date», on behalf of «Company». As you know, 15 U.S.C. §4403(a)(A) of the Comprehensive Smokeless Tobacco Health Education Act provides in part that each person who manufactures, packages, or imports smokeless tobacco products shall annually provide the Department of Health and Human Services with a list of the ingredients added to tobacco in the manufacture of smokeless tobacco products as well as a specification of the quantity of nicotine contained in each product.


An initial review of the submission reveals that the Ingredient Report contains errors as summarized in the attached document. Federal Register notice 50 FR 49617, December 3, 1985, specifies that the ingredient submission “shall be provided reporting each ingredient by chemical name and chemical abstract service (CAS) registry number.” Please correct the errors and provide a written update within 60 business days. Upon receipt of your corrected Ingredient Report, CDC will complete its review of your submission and provide a final determination regarding compliance.



If you require additional assistance please contact Ruth L. Hayes, (770) 488-5743.


Sincerely yours,



Tim A. McAfee, MD, MPH

Director

Office on Smoking and Health

National Center for Chronic Disease Prevention and Health Promotion


Enclosure: (1)


Public reporting burden of this collection of information is estimated to average 6.5 hours per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing the collection of information. An agency may not collect or sponsor and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden, to CDC/ATSDR Reports Clearance Officer, 1600 Clifton Road NE, MS D-74, Atlanta, Georgia 30333; ATTN: PRA (0920-0338).

File Typeapplication/msword
File TitleRequest for OMB Clearance
Authoraph6
Last Modified Byaro5
File Modified2013-09-12
File Created2013-09-12

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