Banda-sil Liquid Gel
FDA Label NDC 72363-005

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ag Essence Inc for the product Banda-sil Liquid Gel (NDC 72363-005). 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 dosage & administration, warnings, inactive ingredient, indications & usage, otc - keep out of reach of children, otc - purpose, otc - active ingredient, banda-sil spray gel box, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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