要依据美国食榀、药榀、化让路法案501款以及美国药典和国家处方集的各论中的含量测定和质量标准来构建法定标准。
According to Section 501 of the Federal Food Drug and Cosmetic Act assays and specifications in monographs of the United States Pharmacopeia and the National Formulary constitute legal standards.
用户必须确认在除《美国药典-国家处方集》，《食品化学法典》或《膳食补充剂法典》之外使用US P标准品的适用性。
Users must determine the suitability of Reference Standards for applications and USES not in the usp-nf, Food Chemicals Codex, or Dietary Supplements Compendium.
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