Antibacterial Hand Sanitizer
FDA Label NDC 90121-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sweda Company Llc for the product Antibacterial Hand Sanitizer (NDC 90121-003). 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, uses, warnings:, when using this product,, stop use and ask a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 62%
Purpose
Antiseptic
Uses
For hand washing to decrease bacteria on the skin.
Warnings:
Flammable. Keep away from fire or flame. For External use only
When Using This Product,
keep out of eyes. In case of contact with eyes, rinse with water.
Stop Use And Ask A Doctor
if irritation and redness develops and persists.
Keep Out Of Reach Of Children.
If swallowed, get medical help promptly and contact poison Control.
Directions
Wet hands thoroughly with product allow to dry without wiping.
Other Information
Store at 20°C (68°-77°F).
Inactive Ingredients:
Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl acetate, Triethanolamine, Water.
Package Labeling:120Ml
Label3 (Label3)
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