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Verification of regulatory compliance is essential before initiating treatment, and healthcare providers must ensure adherence to applicable federal, state, and local regulations

OINDP stands for Orally Inhaled and Nasal Drug Products the regulatory category used by the FDA to classify both inhalation products (metered-dose inhalers, dry powder inhalers, nebulizers) and nasal drug products (nasal sprays, nasal aerosols)

Topical maintenance is likely necessary regardless of initial delivery method, since the skin continuously turns over collagen

Future research: Its crucial to acknowledge that the majority of these studies have been performed in vitro or on animal subjects