Dosage & Administration
For topical use only
Hand Santizer
FDA Label NDC 74054-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Robert Mazza, Inc Dba Five & 20 Spirits for the product Hand Santizer (NDC 74054-100). 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, otc - active ingredient, inactive ingredient, indications & usage, otc - keep out of reach of children, otc - purpose, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Alcohol - 80%ABV
Inactive Ingredient
Glycerin, Hydrogen Peroxide, Water
Indications & Usage
For external use only
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
Otc - Purpose
Sanitizer - for hands
Warnings
For external use only, flammable, keep away from heat or flame.
Package Label.Principal Display Panel
Label (Label)
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