Calmodulin (CaM) regulates steady-state inactivation of sodium currents (Na_V1.4) in skeletal muscle. Defects in Na current inactivation are associated with pathological muscle conditions such as myotonia and paralysis. The mechanisms of CaM modulation of expression and function of the Na channel are incompletely understood. A physical association between CaM and the intact C terminus of Na_V1.4 has not previously been demonstrated. FRET reveals channel conformation-independent association of CaM with the C terminus of Na_V1.4 (CT-Na_V1.4) in mammalian cells. Mutation of the Na_V1.4 CaM-binding IQ motif (Na_V1.4_IQ/AA) reduces cell surface expression of Na_V1.4 channels and eliminates CaM modulation of gating. Truncations of the CT that include the IQ region abolish Na current. Na_V1.4 channels with one CaM fused to the CT by variable length glycine linkers exhibit CaM modulation of gating only with linker lengths that allowed CaM to reach IQ region. Thus one CaM is sufficient to modulate Na current, and CaM acts as an ancillary subunit of Na_V1.4 channels that binds to the CT in a conformation-independent fashion, modulating the voltage dependence of inactivation and facilitating trafficking to the surface membrane.