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A **combination injectable kit product** containing **isopropyl alcohol** for skin antisepsis before injection, **lidocaine hydrochloride** as a local anesthetic to reduce procedural pain, and **methylprednisolone** as the principal therapeutic agent. The pharmacologically dominant component is methylprednisolone, a synthetic glucocorticoid that activates the glucocorticoid receptor to suppress inflammatory gene expression and broad immune signaling; lidocaine contributes reversible local sodium-channel blockade at the administration site, while isopropyl alcohol serves a preparatory antiseptic role rather than a systemic therapeutic one. Based on the provided context, this product appears to correspond to an unapproved combination presentation related to office-based corticosteroid injection products rather than a distinct globally established INN-branded asset, and the labeling context indicates it has not been found by FDA to be safe and effective and has not had FDA-approved labeling.
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