Pureza Advanced Hand Sanitizer
FDA Label NDC 81182-000

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Industrias Coramodio C.a for the product Pureza Advanced Hand Sanitizer (NDC 81182-000). 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 if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Uses

  • Hand sanitizer to help reduce bacteria on the skin that could cause disease 
  • Recommended for repeated use

Warnings

Flammable. keep away from fire or flame.
For external use only

When Using This Product

do not use in or near the eyes. In case of contact, rinse eyes throroughly with water.

Stop Use And Ask A Doctor If

irritation or rash appears os ojos con agua. and lasts

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product in your palm to thoroughly cover your hands • Rub hands together briskly until dry • No rinsing required • No towels needed

Other Information

• Store below 110°F (43°C)
• May discolor certain fabrics or surfaces

Inactive Ingredients

Alcohol, Water, Isopropyl Alcohol, Glycerin, Carbomer, Triethanolamine, Fragance.

Package Labeling:80Ml

Label (Label)

Label (Label)

Package Labeling:200Ml

Bottle2 (Bottle2)

Bottle2 (Bottle2)

Package Labeling:500Ml

Bottle3 (Bottle3)

Bottle3 (Bottle3)

Package Labeling:1000Ml

Bottle4 (Bottle4)

Bottle4 (Bottle4)

Package Labeling:3780Ml

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