Preatorian Hand Sanitizer
FDA Label NDC 80455-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sistema Corporativo Deutzia, S.a. De C.v. for the product Preatorian Hand Sanitizer (NDC 80455-000). 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 ingredients, purpose, uses., warning, when using this product:, stop use and ask of a doctor if:, 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 Ingredients
Ethyl alcohol 70%
Purpose
Anticeptic
Uses.
To decrease bacteria on the skin that could cause disease. Recommended for repeated use.
Warning
For external use only: HANDS. Flammable, keep away from fire or flame.
When Using This Product:
keep out eyes, in case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. don´t inhale or ingest.
Stop Use And Ask Of A Doctor If:
Irritation and redness develop. condition persists 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
We hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult
supervision. Not recommended for infants.
Other Information
Don´t store above 105°F. may discolor some fabrics. harmful to wood finishes and plastics
Inactive Ingredients
Water, Carbomer, Triethanolamine, Alkylating, Agent, Aloe.
Package Labeling:125Ml
Label (Label)
Package Labeling:250Ml
Label2 (Label2)
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