FDA WARNING_LETTER - Ten Days Manufacturing d/b/a Daily Manufacturing - April 01, 2026

On April 21, 2026, the U.S. Food and Drug Administration (FDA) issued a warning letter to Daily Manufacturing Solutions Inc., located in Rancho Cucamonga, California. Following a review of inspection records, the FDA determined that the company manufactures and distributes nicotine pouch products, such as "PUCK COOL MINT 6MG," without the necessary legal authorization. Under the Federal Food, Drug, and Cosmetic Act, any tobacco product that was not on the market before February 15, 2007, is considered a "new tobacco product" and requires a premarket authorization order to be legally sold in the United States. Because Daily Manufacturing Solutions Inc. failed to obtain this authorization or submit required reports, their products are classified as both adulterated and misbranded. The FDA has directed the company to take immediate action to address these violations and ensure all products and marketing materials comply with federal regulations. The company must provide a written response within 15 working days detailing the steps taken to correct these issues, including the dates they stopped selling the unauthorized products and their plan for future compliance. Failure to comply may result in serious regulatory consequences, such as fines, product seizures, or court-ordered injunctions.