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What it does is initiate a formal rulemaking process under the Federal Food, Drug, and Cosmetic Act in which the FDA must publish a proposed rule, accept public comment typically for 60 to 90 days and issue a final determination

Treat the schedule above as reported use, not a recommendation

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Use this break to: Assess baseline sleep quality without DSIP Allow any potential receptor adaptation to normalize Evaluate whether continued use is necessary or beneficial If returning to DSIP after the break, you may find your effective dose has changed