Otc - Active Ingredient
Alcohol (62%)
Hand Sanitizer
FDA Label NDC 19392-110
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bullet Line, Llc for the product Hand Sanitizer (NDC 19392-110). 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, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, 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
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
Indications & Usage
For 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
Dosage & Administration
Recommended for repeated use
Inactive Ingredient
Water, Hydrogenated starch, Carbomer, Tetrahydroxypropyl Ethylenediamine, Fragrance
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