Remeverse Instant Foam Hand Sanitizer
FDA Label NDC 70317-145

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Remeverse for the product Remeverse Instant Foam Hand Sanitizer (NDC 70317-145). 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 remeverse instant foam hand sanitizer, topical antimicrobial, benzalkonium chloride .1% active, warnings:, safety warning, warning - children, purpose - antimicrobial, label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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