Contact:
| David K. Waldman/John W. Heilshorn |
The Quigley Corporation |
| Lippert Heilshorn & Associates |
Carl Fonash |
| (212) 838-3777 |
Shareholder Relations |
| dwaldman@lhai.com |
(267) 880-1111 |
Quigley Completes Purchase of Manufacturing Assets of JOEL
DOYLESTOWN, PA. - October 5, 2004 - The Quigley Corporation (Nasdaq: QGLY) has completed the asset purchase with JOEL, Inc., as announced on August 20,
2004, for approximately $5.1 million, which includes $4.1 million in cash and
$1.0 million of the Company's stock. The transfer of assets includes inventory,
as well as land, buildings, machinery and equipment of two manufacturing
facilities, located in Lebanon and Elizabethtown, Pennsylvania.
The Company funded the acquisition through its current working capital of $1.1
million and financed $3.0 million of the cash requirement through a 7-year term
loan with PNC Bank, N.A., a Pennsylvania commercial bank.
JOEL, Inc. has been the exclusive manufacturer of the Company's ColdEEZE®
Lozenge since its launch in 1995.
The Quigley Corporation (Nasdaq: QGLY, http://www.Quigleyco.com) is a leading
developer and marketer of diversified health products including the
COLD-EEZE® family of patented zinc gluconate glycine (ZIGG) lozenges
and sugar free tablets. COLD-EEZE is the only (ZIGG) lozenge proven in two
double-blind studies to reduce the duration of the common cold from 7.6 to 4.4
days or by 42%. In addition to Over-The-Counter (OTC) products, the Company has
formed Quigley Pharma Inc. (http://www.QuigleyPharma.com), a wholly owned
ethical pharmaceutical subsidiary, to introduce a line of naturally-derived
patented prescription drugs. The Quigley Corporation's customers include
leading national wholesalers and distributors, as well as independent and chain
food, drug and mass merchandise stores and pharmacies. The Quigley Corporation
makes no representation that the U.S. Food and Drug Administration or any other
regulatory agency will grant an IND or take any other action to allow the
aforementioned products to be studied or marketed. Furthermore, no claim is
made that the potential medicine discussed here is safe, effective, or approved
by the Food and Drug Administration.
Certain statements in this press release are "forward-looking
statements" within the meaning of the Private Securities Litigation Reform
Act of 1995 and involve known and unknown risk, uncertainties and other factors
that may cause the company's actual performance or achievements to be
materially different from the results, performance or achievements expressed or
implied by the forward-looking statement. Factors that impact such
forward-looking statements include, among others, changes in worldwide general
economic conditions, changes in interest rates, government regulations, and
worldwide competition.
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