Frequently Asked Questions

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FAQs About the Regulation of OTC Medicines

Browse commonly asked questions about over-the-counter medicines and how they are regulated within the United States.

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FAQs About Dietary Supplements Regulations

Regulation of Dietary Supplements covers marketing, manufacturing, labeling, and advertising enforced by FDA and the Federal Trade Commission. See these FAQs to learn more.

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FAQs

FAQs About Manufacturing Quality

Learn about how CHPA member companies ensure that OTC medicine quality is standardized across the U.S.

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FAQs

FAQs About Dextromethorphan
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FAQs

FAQs About OTC Monograph Reform for Manufacturers
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FAQs

FAQs About Drug Distribution in the United States
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FAQs

FAQs About Homeopathic Medicine

Learn about the uses, safety, and regulation of homeopathic medicines in the U.S.

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FAQs

FAQs About the OTC Review

Learn about the OTC review process, drug monographs, and time and extent applications.

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FAQs

FAQs About Acetaminophen and Other Oral OTC Pain Relievers and Fever Reducers

Find frequently asked questions about OTC oral pain relievers and fever reducers including acetaminophen, aspirin, ibuprofen, ketoprofen, and naproxen sodium.

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FAQs

FAQs About Rx-to-OTC Switch

Learn about the process of transferring FDA-approved prescription medications to nonprescription, over-the-counter status.

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FAQs

FAQs About Consumer Medical Devices
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FAQs

FAQs About Reforms to the OTC Monograph System
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FAQs

FAQs About HSA/FSA Accounts and the CARES Act
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FAQs

FAQs About Standardized Information on Dietary Ingredients (SIDI)

Find frequently asked questions about the Standardized Information on Dietary Ingredients (SIDI).

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