Mayo Hygiene Instant Hand Sanitizer
FDA Label NDC 75809-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Cuifu Cosmetics Co., Ltd for the product Mayo Hygiene Instant Hand Sanitizer (NDC 75809-000). 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 active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor, keep out of reach of children., directions, 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

A Hand Sanitizer to help reduce bacteria that potentially can cause disease. Recommended for repeated use. For use when soap and water are not available.

Warnings

For external use only.

Flammable. Keep away from heat or flame.

When Using This Product

do not use in or near eyes,ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor

if irritation or rash appears on the skin.

Keep Out Of Reach Of Children.

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

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Children under 6 years of age should be supervised by adult when applying this product.
  • Do not use on children less than 2 months of age or on open skin wounds.

Other Information

Do not store above 40C(104F). May discolor some fabrics or surfaces.

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Carbomer, Glycerin, Water.

Package Labeling:

Bottle (Bottle)

Bottle (Bottle)

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