Otc - Active Ingredient
Ethanol (71%)
Hand Sanitizer
FDA Label NDC 19392-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Humphreyline for the product Hand Sanitizer (NDC 19392-100). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, inactive ingredient, otc - keep out of reach of children, dosage & administration, 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 - Purpose
Antimicrobial
Indications & Usage
Hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.
Warnings
For external use only. Keep out of eyes. Keep out of reach of children. Flammable-keep away from open flame.
Inactive Ingredient
Purified water, isopropanol, glycerin, glycerol monolaurate
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
Dosage & Administration
Recommended for repeated use
Package Label.Principal Display Panel
Pen Spray Art (Penspray)
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