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Nope! All of our products are NDC compliant and are safe for purchase and use at home.

An NDC registered over-the-counter health product refers to an over-the-counter medication or health product that has been assigned a unique National Drug Code by the U.S. Food and Drug Administration (FDA). The NDC is a 10-digit, three-segment number that identifies the product's manufacturer, the product itself, and the package size. This code is crucial for tracking and identifying specific products, ensuring accurate labeling, and assisting in the reporting and monitoring of adverse events associated with the product.

The NDC can usually be found on the packaging or label of the over-the-counter health product. Look for a 10-digit number divided into three segments with hyphens, for example, 12345-6789-10. The first segment represents the product's labeler code (the manufacturer or distributor), the second segment denotes the product code (specific drug or combination), and the third segment signifies the package size and type.

Yes, all over-the-counter health products that are sold in the United States and regulated by the FDA are required to have an NDC registration. Using NDC registered products ensures that the product has undergone regulatory scrutiny, is accurately labeled, and has been assigned a unique identifier to facilitate tracking and safety monitoring. Additionally, healthcare providers, consumers, and manufacturers benefit from the ability to easily identify and differentiate specific products, reducing the risk of medication errors and enhancing patient safety.