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Looking for 118-56-9 / Homosalate API manufacturers, exporters & distributors?

Homosalate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Homosalate 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 Homosalate manufacturer or Homosalate supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Homosalate manufacturer or Homosalate supplier.

PharmaCompass also assists you with knowing the Homosalate API Price utilized in the formulation of products. Homosalate API Price is not always fixed or binding as the Homosalate Price is obtained through a variety of data sources. The Homosalate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Homosalate

Synonyms

118-56-9, Homomenthyl salicylate, 3,3,5-trimethylcyclohexyl salicylate, Coppertone, Heliopan, Heliophan

Cas Number

118-56-9

Unique Ingredient Identifier (UNII)

V06SV4M95S

About Homosalate

Homosalate is an organic compound that belongs to salicylates. It is an ester formed from salicylic acid and 3,3,5-trimethylcyclohexanol, a derivative of cyclohexanol. Salicylates prevent direct skin exposure to the suns harmful rays by absorbing ultraviolet (UV) light. Homosalate specifically absorbs short-wave UVB rays, which are associated with DNA damage and increased risk of skin cancer. It is a common ingredient in many commercially available sunscreens. There are no reported adverse effects from homosalate.

MolPort-001-793-236 Manufacturers

A MolPort-001-793-236 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-793-236, including repackagers and relabelers. The FDA regulates MolPort-001-793-236 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-793-236 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 MolPort-001-793-236 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-793-236 Suppliers

A MolPort-001-793-236 supplier is an individual or a company that provides MolPort-001-793-236 active pharmaceutical ingredient (API) or MolPort-001-793-236 finished formulations upon request. The MolPort-001-793-236 suppliers may include MolPort-001-793-236 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-793-236 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-793-236 GMP

MolPort-001-793-236 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 MolPort-001-793-236 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 MolPort-001-793-236 GMP manufacturer or MolPort-001-793-236 GMP API supplier for your needs.

MolPort-001-793-236 CoA

A MolPort-001-793-236 CoA (Certificate of Analysis) is a formal document that attests to MolPort-001-793-236's compliance with MolPort-001-793-236 specifications and serves as a tool for batch-level quality control.

MolPort-001-793-236 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-001-793-236 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.

MolPort-001-793-236 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-001-793-236 EP), MolPort-001-793-236 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-001-793-236 USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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