Mynt Naturals Hand Sanitizer Ultra Moisturizing
FDA Label NDC 79442-101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Prive International Inc. for the product Mynt Naturals Hand Sanitizer Ultra Moisturizing (NDC 79442-101). 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 drug facts, active ingredient, purpose, indications & usage, otc - keep out of reach of children, dosage & administration, storage and handling, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Drug Facts

→ Active Ingredient

→ Purpose

→ Indications & Usage

→ Otc - Keep Out Of Reach Of Children

→ Dosage & Administration

→ Storage And Handling

→ Packaging

Drug Facts

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Indications & Usage

Uses - To decrease bacteria on the skin that could cause disease - Recommended for repeated use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

Directions - wet hands thoroughly with product and allow to dry without wiping - for children under 6, use only under adult supervision - not recommended for infants.