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1. Mundasal
2. Mundisal
1. 2016-36-6
2. Syrap
3. (2-hydroxyethyl)trimethylammonium Salicylate
4. Choline Salicylic Acid Salt
5. Salicylic Acid Choline Salt
6. Choline, Salicylate (salt)
7. Cholin Salicylate
8. Salicylic Acid, Ion(1-), Choline
9. Choline Subsalicylate
10. 2-hydroxy-n,n,n-trimethylethanaminium 2-hydroxybenzoate
11. Ethanaminium, 2-hydroxy-n,n,n-trimethyl-, Salt With 2-hydroxybenzoic Acid (1:1)
12. Kd510k1iqw
13. Arthropan
14. 2-hydroxy-n,n,n-trimethylethanaminium Salt With 2-hydroxybenzoic Acid (1:1)
15. Actasal
16. Artrobione
17. Mundisal
18. Salicol
19. Satibon
20. Arret
21. 2-hydroxybenzoate;2-hydroxyethyl(trimethyl)azanium
22. 2-carboxyphenolate;2-hydroxyethyl(trimethyl)azanium
23. Choline Salicylate B
24. Cholinesalicylate
25. Ethanaminium, 2-hydroxy-n,n,n-trimethyl-, 2-hydroxybenzoate (1:1)
26. Cholini Salicylas
27. Salicilato De Colina
28. Cholini Salicylas [inn-latin]
29. Salicylate De Choline
30. Salicilato De Colina [inn-spanish]
31. Salicylate De Choline [inn-french]
32. Einecs 217-948-8
33. Unii-kd510k1iqw
34. Choline Salicylate [usan:inn:ban:jan]
35. Arthropan (tn)
36. Choline Salicylate (salt)
37. Schembl3960
38. Chebi:3668
39. Choline Salicylate [mi]
40. Chembl2104095
41. Choline Salicylate [inn]
42. Choline Salicylate [jan]
43. Dtxsid8062103
44. Choline Salicylate [usan]
45. Choline Salicylate [vandf]
46. Choline Salicylate [mart.]
47. Choline Salicylate [who-dd]
48. Choline Salicylate (jan/usan/inn)
49. Mfcd00242760
50. Akos030228339
51. Db14006
52. As-66082
53. Cs-0449641
54. D00810
55. (2-hydroxyethyl)trimethylazanium 2-hydroxybenzoate
56. A909239
57. (2-hydroxyethyl)trimethyl Ammonium Salicylate
58. 2-carboxyphenolate,2-hydroxyethyl(trimethyl)azanium
59. Q4499058
60. (2-hydroxyethyl)trimethylammonium 2-hydroxybenzoate
61. 2-hydroxy-n,n,n-trimethylethan-1-aminium 2-hydroxybenzoate
62. 2-hydroxy-n,n,n-trimethylethan-1-aminium 2-carboxyphenolate
63. Benzoic Acid, 2-hydroxy-, Ion(1-), 2-hydroxy-n,n,n-trimethylethanaminium
Molecular Weight | 241.28 g/mol |
---|---|
Molecular Formula | C12H19NO4 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 3 |
Exact Mass | 241.13140809 g/mol |
Monoisotopic Mass | 241.13140809 g/mol |
Topological Polar Surface Area | 80.6 Ų |
Heavy Atom Count | 17 |
Formal Charge | 0 |
Complexity | 179 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
The oral gel is indicated for the relief of pain and discomfort of common mouth ulcers, cold sores, denture sore spots, infant teething and mouth ulcers, and sore spots due to orthodontic devices in children.
This is an anti-inflammatory and antipyretic medication,. If is often used in oral gel form for the relief of pain, discomfort, and inflammation caused by common mouth ulcers, cold sores, denture and sore spots, as well as mouth ulcers, and sore spots because of orthodontic devices.
N - Nervous system
N02 - Analgesics
N02B - Other analgesics and antipyretics
N02BA - Salicylic acid and derivatives
N02BA03 - Choline salicylate
Absorption
Onset: 1-2 hr after ingestion In the oral form, choline salicylate is absorbed across the buccal mucosa. There is a need for caution not to exceed the stated dose and monitor for any signs of suggested salicylism, especially when this drug is used for infants. In one study, it was found that this drug was more rapidly absorbed than ASA (absorption t1/2 = 0.1 vs 0.36 h).
Route of Elimination
Both metabolites of choline salicylate, and a small amount of intact salicylic acid are excreted, primarily in the urine.
Volume of Distribution
0.15 L/kg (salicylate), and widely distributed throughout extracellular water and most tissues
The metabolism of salicylic acid is by glycine and phenolic or acyl glucuronate conjugation with small amounts of the drug undergoing hydroxylation. Extensively metabolized in the liver; inactive metabolites are excreted by the kidneys.
The plasma half-life of salicylic acid is 2-4 hours. Up to 15 30 h with larger doses due to saturation of liver metabolism capacity.
Choline salicylate relieves pain by inhibition of prostaglandin synthesis and reduces fever by acting on the hypothalamus heat-regulating center. It also inhibits the generation of impulses through the inhibition of cyclooxygenase enzyme (COX),. Cyclooxygenase is involved in the production of prostaglandins, in response to injury and after various other stimuli. The prostaglandins promote pain, swelling, and inflammation. The choline salicylate decreases inflammation and pain by reducing the production of these prostaglandins in the area of the mouth it is applied to.
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PharmaCompass offers a list of Choline Salicylate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Choline Salicylate manufacturer or Choline Salicylate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Choline Salicylate manufacturer or Choline Salicylate supplier.
PharmaCompass also assists you with knowing the Choline Salicylate API Price utilized in the formulation of products. Choline Salicylate API Price is not always fixed or binding as the Choline Salicylate Price is obtained through a variety of data sources. The Choline Salicylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Salicilato de colina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Salicilato de colina, including repackagers and relabelers. The FDA regulates Salicilato de colina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Salicilato de colina API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Salicilato de colina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Salicilato de colina supplier is an individual or a company that provides Salicilato de colina active pharmaceutical ingredient (API) or Salicilato de colina finished formulations upon request. The Salicilato de colina suppliers may include Salicilato de colina API manufacturers, exporters, distributors and traders.
click here to find a list of Salicilato de colina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Salicilato de colina DMF (Drug Master File) is a document detailing the whole manufacturing process of Salicilato de colina active pharmaceutical ingredient (API) in detail. Different forms of Salicilato de colina DMFs exist exist since differing nations have different regulations, such as Salicilato de colina USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Salicilato de colina DMF submitted to regulatory agencies in the US is known as a USDMF. Salicilato de colina USDMF includes data on Salicilato de colina's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Salicilato de colina USDMF is kept confidential to protect the manufacturer’s intellectual property.
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A Salicilato de colina written confirmation (Salicilato de colina WC) is an official document issued by a regulatory agency to a Salicilato de colina manufacturer, verifying that the manufacturing facility of a Salicilato de colina active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Salicilato de colina APIs or Salicilato de colina finished pharmaceutical products to another nation, regulatory agencies frequently require a Salicilato de colina WC (written confirmation) as part of the regulatory process.
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National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Salicilato de colina as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Salicilato de colina API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Salicilato de colina as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Salicilato de colina and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Salicilato de colina NDC to their finished compounded human drug products, they may choose to do so.
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Salicilato de colina Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Salicilato de colina GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Salicilato de colina GMP manufacturer or Salicilato de colina GMP API supplier for your needs.
A Salicilato de colina CoA (Certificate of Analysis) is a formal document that attests to Salicilato de colina's compliance with Salicilato de colina specifications and serves as a tool for batch-level quality control.
Salicilato de colina CoA mostly includes findings from lab analyses of a specific batch. For each Salicilato de colina CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Salicilato de colina may be tested according to a variety of international standards, such as European Pharmacopoeia (Salicilato de colina EP), Salicilato de colina JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Salicilato de colina USP).