Replacing graphite anodes with Si anodes can greatly increase the capacity of current Li-ion batteries. Detailed characterization of Si lithiation reactions, solid electrolyte interphase (SEI) formation, and reversibility are therefore active areas of research. Solid-state nuclear magnetic resonance (NMR) spectroscopy is useful for characterizing different local environments within Si anodes as well as differentiating surface and bulk environments. Furthermore, non-invasive and non-destructive NMR methods can reveal metastable LixSi phases or SEI species forming on (dis)charge that may be too reactive to detect via ex situ methods. Here, we use an in situ and in operando NMR methodology to characterize full pouch cells comprising of Si anodes and NMC cathodes. We can observe changes in the relative amounts of Li in different environments within the same Si anode before/during/after charge & discharge and with various amounts of cycling or calendar aging using in situ 7Li NMR. The pouch cells used in our in situ NMR study are comparable to pouch cells made using mid- to large-scale fabrication methods as opposed to laboratory scale; in other words, challenges of cell-to-cell variability are minimized. We hypothesize “trapped” lithiated phases formed in the Si anode no longer contribute to electrochemical cycling and thus limit capacity in subsequent cycles/aging. We also characterized the SEI/surface species in situ with aging via 13C NMR measurements, identifying reactions of lithium silicides with electrolyte solvents and their subsequent decomposition.