Neuropathy Pain Relief Cream
FDA Label NDC 83570-002

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Owell Naturals Brand, Llc for the product Neuropathy Pain Relief Cream (NDC 83570-002). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding purpose, active ingredient, using, question?, warnings, direction, inactive ingredent, indications, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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