Otc - Active Ingredient
Ethyl Alcohol (63%)
Hand Sanitizer
FDA Label NDC 19392-130
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 19392-130). 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 sanitizer to help reduce bacteria on the skin
Warnings
For external use only. Do not use in or near the eyes. Stop use and ask a doctor if irritation or rash appears and lasts. Keep out of reach of children. If swallowed contact a doctor or Poison Control Center right away. Flammable-keep away from open flame.
Inactive Ingredient
Water, Glycerin, Aloe Vera Leaf Extract, Citrus Peel Extract
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed contact a doctor or Poison Control Center right away.
Dosage & Administration
Wet hands thoroughly with product and allow to dry without wiping.
Package Label.Principal Display Panel
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