Bevoline
FDA Label NDC 70013-302

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Skin Divine Inc. for the product Bevoline (NDC 70013-302). 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 statement of identity, otc - active ingredient, warnings, otc - ask doctor/pharmacist, otc - when using, otc - stop use, instructions for use, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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