Hand Sanitizer
FDA Label NDC 78153-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Quimi Clean for the product Hand Sanitizer (NDC 78153-000). 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 70%
Purpose
Antiseptic
Uses
to decrease bacteria on the skin that could cause disease recommended for repeated use.
Warnings
For external use only: hands
Flammable, keep away from fire or flame
When Using This Product
keep out of eyes, In case of contact with eyes, flush thoroughly with water./ avoid contact with broken skin/ do not inhale or ingest.
Stop Use And Ask A Doctor
of irritation and redness develop/ condition persosts for more than 72 hours
Keep Out Of Reach Of Children
if swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wet hands thorouughly with product and allow to dry without wiping / for children under 6, use only under adult supervision/ not recommended for infacts
Other Information
do not store above 105 F / may discolor some fabrics / harmful to wood finishes and plastics
Inactive Ingredients
Water, glycerin/caprylate carbopol, vitamin E,Water, glycerin, caprate, tocopheryl acetate, acrylates/C10-30 alkyl acrylates crosspolymer
Package Labeling:240Ml
Bottle (Bottle)
Package Labeling:400Ml
Bottle2 (Bottle2)
Package Labeling:580Ml
Bottle3 (Bottle3)
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