patent medicine
patent medicine packaged drugs that can be obtained without prescription; the term was formerly used to describe quack remedies sold by peddlers. Patent, or proprietary, medicines are advertised to the public by trade name, purport to be effective against minor disorders and symptoms, and are packaged with directions for use. Antiseptics , analgesics , some sedatives , laxatives , and antacids , cold and cough medicines, and various skin preparations are included in the group. Sale of proprietary medicines is regulated by the Food and Drug Administration, which evaluates preparations as to their safety and effectiveness.
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The U.S. Food and Drug Administration.(Business News)(Brief Article)
Magazine article from: Security Management; 9/1/2003; 27 words
; The U.S. Food and Drug Administration has granted 510(k) clearance to American Bio Medica Corporation for a drug testing technology to detect propoxyphene (trade name: Darvon).
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Complaint Filed With FDA Against RU486.(United States Food and Drug Administration abortion drug)(Evaluation)
Magazine article from: National Right to Life News; 9/1/2002; 700+ words
; ...Citizen Petition filed with the Food and Drug Administration is asking the FDA to rescind its approval...dangerousness of Mifeprex [RU486's U.S. trade name] by inappropriately resorting to the...manufacturer of misoprostol (sold under the trade name Cytotec), however, never filed an ...
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Food and Drug Administration.
Magazine article from: Healthcare Purchasing News; 11/1/1999; 111 words
; ...equipment will work properly on Jan. 1, 2000, the Food and Drug Administration and medical device associations assured members of two...question the degree of industry compliance. The Food and Drug Administration is responsible for oversight and regulation of medical...
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Ex-head of China's FDA receives death sentence for taking bribes.(International)(Food and Drug Administration)
Magazine article from: Adverse Event Reporting News; 6/4/2007; 700+ words
; ...former chief of the State Food and Drug Administration, was not unprecedented in China...replaced as head of the State Food and Drug Administration in 2005, seemed aimed more at the...Despite approval by the State Food and Drug Administration, it killed at least six people and...
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Food & Drug Administration.(Grapevine: news about people ...)(United States. Food and Drug Administration)(policy planner resignation)(Brief Article)
Newspaper article from: Food & Drink Weekly; 3/21/2005; 190 words
; Food & Drug Administration chief policy planner William Hubbard has announced his retirement. Dr. Randall Lutter, the chief economist in FDA's Office of Planning...
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The Food and Drug Administration (FDA).(Marketing News)
Magazine article from: Household & Personal Products Industry; 3/1/2004; 35 words
; The Food and Drug Administration (FDA) approved Tri-Active LaserDermology to treat cellulite. It incorporates mechanical massage, localized cooling and deep laser stimulation. It smoothes and tightens the outer layers of skin.
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Series of mix-ups leads to turmoil over a trade name.(FaciliClean LLC)
Magazine article from: New Hampshire Business Review; 8/17/2007; ; 700+ words
; How did FaciliClean LLC, a trade name reserved and registered by Ed Tyler for...division since 1994. Duprey registered the trade name it was operating under--Facilitech--with...Oct. 17, Tyler had already reserved the trade name FaciliClean at the Secretary of State...
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FDA issues final bar coding rule for drugs and blood.(Policy Watch)(Food and Drug Administration)(Brief Article)
Magazine article from: Healthcare Financial Management; 4/1/2004; 215 words
; On February 25, the Food and Drug Administration (FDA) issued a final rule requiring bar codes on most...hospitals or nursing homes to implement new automated drug administration systems; however, the requirements are expected to...
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Food and Drug Administration.(removed the "unit-of use" packaging requirement for dietary supplements and drug products with 30 milligrams or more of iron per dosage)(Brief Article)
Magazine article from: Food & Drug Packaging; 12/1/2003; 41 words
; The Food and Drug Administration has removed the unit-of use packaging requirement for dietary supplements and drug products with 30 milligrams or more of iron per dosage. The accidental overdose warning and child-resistant packaging requirements remain in effect.
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Food and Drug Administration.(Personnel Roundup)
Magazine article from: Household & Personal Products Industry; 7/1/2005; 73 words
; Food and Drug Administration: Sheldon T. Bradshaw has been named as the new associate general counsel of the food and drug division of the office of the general...
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The Germ Theory and Patent Medicine
Book article from: American Eras
The Germ Theory and Patent Medicine Unregulated Medicines. In the...invent one and try to sell it. Patent medicines got their name because their...Cure-All. ” Manufacturers of patent medicines typically claimed that they...
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Patent-Medicine Advertisements
Book article from: American Decades
PATENT-MEDICINE ADVERTISEMENTS The Poison Trust The...a total of $59 million each year on patent medicines. More of that money went to pay the...magazine would no longer accept ads for patent medicines. By 1904, when the industry's success...
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1783-1815: Charlatans and Patent Medicines
Book article from: American Eras
Charlatans and Patent Medicines Patent Medicines . Colonial Americans had imported from England a variety of patent medicines (so called because they had...that “ the venders of patent medicines in almost every capital town...
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patent medicine
Book article from: The Oxford Pocket Dictionary of Current English
pat·ent med·i·cine • n. a proprietary medicine made and marketed under a patent and available without prescription.
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The Patent Office
Book article from: American Eras
...had invented the steamboat. Thornton refused to grant a patent to John Hall, the inventor of the breech-loading rifle...Thornton ’ s death in 1828, Congress reorganized the Patent Office, requiring stricter examination of patents (for example, it was no longer possible to patent a ...
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