01 1Hubei Meikai Chemical Co Ltd
02 1MakingCosmetics Inc.
03 1Vantage Specialty Chemicals, Inc.
04 1Yidu Huayang Chemical Co., Ltd. (Zhicheng Factory)
01 2OXYBENZONE
02 2Oxybenzone
01 2China
02 2U.S.A
NDC Package Code : 49464-0001
Start Marketing Date : 2016-06-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61726-109
Start Marketing Date : 2017-12-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 80466-102
Start Marketing Date : 1997-11-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 13317-532
Start Marketing Date : 2011-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Oxybenzone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxybenzone, including repackagers and relabelers. The FDA regulates Oxybenzone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxybenzone API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Oxybenzone supplier is an individual or a company that provides Oxybenzone active pharmaceutical ingredient (API) or Oxybenzone finished formulations upon request. The Oxybenzone suppliers may include Oxybenzone API manufacturers, exporters, distributors and traders.
click here to find a list of Oxybenzone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Oxybenzone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oxybenzone 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 Oxybenzone 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 Oxybenzone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oxybenzone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oxybenzone suppliers with NDC on PharmaCompass.
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