1. PEG is also used as an excipient in many pharmaceutical products.

2. Each tube contains 15% Amygdalin 10% DMSO (Dimethyl Sulfoxide) and excipient

3. Microcrystalline Cellulose is a commonly used excipient in the pharmaceutical industry

4. The compositions may also contain an amino acid or human albumin as an excipient.

5. According to M & B and RPR, this latter condition includes both active ingredients and excipients.

6. Hypersensitivity to the active substance, to the pre-admixtures or to any of the excipients

7. A gastroretentive composition comprises a mixture comprising an active ingredient component and an excipient component.

8. Excipients: metacresol, sodium dihydrogen phosphate dihydrate, glycerol, sodium hydroxide, hydrochloric acid (for pH adjustment), water for injections

9. Normally, a pharmacologically inactive ingredient (excipient) termed a binder is added to help hold the tablet together and give it strength.

10. The spray-dried products were a mixture of aminopyrine-Barbital complex (molecular ratio 1:1), aminopyrine, and the excipient used

11. Methyl Alcohol, Anhydrous is a colorless, flammable substance used in labs as a solvent excipient for pharmaceutical, cosmetic, personal care and nutrition products

12. The global Biopharmaceutical excipients market size is expected to reach USD 3.4 billion by 2028, according to a new report by Grand View Research, Inc

13. Alaria Surpeme™ is packaged in a bottle of 90 veggie caps, each containing approximately 485 mg of Alaria esculenta without fillers, binders or excipients

14. This form which is preferably a tablet, comprises the active agent(s) in admixture with the above excipient in such an amount as to achieve the requested sustained release.

15. A pharmaceutical formulation comprising an anti-obesity agent, such as sibutramine, and at least one acidulant, such as fumaric acid, together with a pharmaceutically acceptable carrier, diluent or excipient therefor.

16. NEOSORB® Sorbitol liquid Crystallizing and non-Crystallizing products are widely used excipients as a bulk sweetener and vehicle in liquid dosage forms and as a humectant in semi solids

17. 9 It is not clear whether the anaphylactic shock was caused by menaquinones (Vitamin K or by the excipient, polyethoxylated castor oil, which is included in the formulation.

18. Suboxone is contraindicated in the following instances: hypersensitivity to buprenorphine, to naloxone, or to any of the excipients, severe respiratory insufficiency, severe hepatic insufficiency, acute alcoholism or delirium tremens

19. Bregma Pharma-Syria Was founded in June 2009 in Damascus, as supplier of pharmaceutical industry requirement of API’s , excipient, machinery, Clinical studies , technical support , Turn key projects and others

20. The Powder Diffraction File contains many subfiles, such as minerals, metals and alloys, pharmaceuticals, forensics, excipients, superconductors, semiconductors, etc., with large collections of organic, organometallic and inorganic reference materials.

21. Special technologies are required to prevent loss of viability and may include freeze drying, selected excipients to control water activity, enteric coating for protection against gastric acidity and microencapsulation.

22. The composition includes, as an active ingredient, a PPAR$g(g) and/or a RXR agonist which upregulates monocyte/m$g(f) CD36 in admixture with a pharmaceutically acceptable carrier, excipient or diluent.

23. The present invention discloses a traditional Chinese medicine preparation for cardio-cerebral blood vessel diseases, it is prepared though extracting danshen and notoginseng by lye , precipitating with alcohol, concentrating, and adding other medicine and excipients.

24. Table using Option 1 and Option 2 applied to acetonitrile in a veterinary medicinal product Component Amount in formulation Acetonitrile content Daily exposure Active substance 0.3 g 800 ppm 0.24 mg Excipient 1 0.9 g 400 ppm 0.36 mg Excipient 2 3.8 g 800 ppm 3.04 mg Veterinary medicinal product 5.0 g 728 ppm 3.64 mg Drugs and Health Products Features Drug Product Database MedEffect Canada - Advisories, Warnings & Recalls Special Access Programme - Drugs Natural Health Products - Monographs Medical Use of Marihuana - Health Care Professionals

25. According to the list of reference terms in the European Pharmacopoeia, drawn up under the aegis of the Council of Europe, (13) an excipient is an auxiliary substance, generally therapeutically inert, and needed for the manufacture, administration or conservation of the active ingredient.

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27. Hypersensitivity to the active substance or to any of the excipients. Patients with significantly compromised cardiac function, e. g., NYHA Class III/IV. Patients receiving systemic steroid therapy, clonidine and H# blocking agents. Patients who have received an allogenic stem cell transplant. During pregnancy. During breast feeding

28. Luveris is contraindicated in the presence of hypersensitivity to gonadotrophins or to any of the excipients, ovarian failure, uncontrolled thyroid or adrenal failure, active untreated tumours of the hypothalamus and pituitary gland, abnormal uterine bleeding of unknown origin, sex hormone-dependent tumours of the reproductive tract and accessory organs, and pregnancy and lactation.

29. Luveris is contraindicated in the presence of hypersensitivity to gonadotrophins or to any of the excipients, ovarian failure, uncontrolled thyroid or adrenal failure, active untreated tumours of the hypothalamus and pituitary gland, abnormal uterine bleeding of unknown origin, sex hormonedependent tumours of the reproductive tract and accessory organs, and pregnancy and lactation.

30. The present invention relates to a natural beef condiment consisting of almost 100% natural originals, and more particularly, to a natural beef condiment consisting of almost 100% natural originals, not including various chemical synthesized additives, excipients, savory taste components and/or consisting of, as a part of the components thereof, vegetable powder produced through a vacuum freeze-drying process.

31. It concerns high viscosity cosmetic compositions to be applied on the skin directly or indirectly via a piece of adhesive fabric fixed on a woman's apparel element. The invention is characterised in that the compositions contain one or several plant extracts with oestrogen activity and a Kigelia africana or Kigelia pinnata plant extract in a toxicologically harmless non-allergenic viscous excipient.

32. The anhydrous tablet of the invention is characterized by the direct dry tabletting, without using water, of a mixture consisting of the active ingredient anhydrous ranitidine hydrochloride, in the crystalline form 'allomorphous Form 1' having a particular purity and stability, and by a global amount of other excipients and adjuvant substances or inert vehicles less than the weight of the active ingredient.