Handeez Instant Hand Sanitizer
FDA Label NDC 71203-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ei Global Group Llc for the product Handeez Instant Hand Sanitizer (NDC 71203-001). 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 ingredients, purpose, warnings, uses, directions, keep out of reach of children., other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Alcohol 70%.

Purpose

Antiseptic

Warnings

Flammable, keep away from fire and flame.

For external use only.

When using this product

  • Do not get into eyes.
  •  If contact occurs, rinse eyes thoroughly with water. 
  • May discolor some fabrics. 

    • Stop use and ask a doctor.

    •  if Irritation and redness develop. 

Uses

Instant Hand Sanitizer Topical 70% Alcohol Solution.

Directions

wet hands thoroughly with product and allow to dry without wiping.

Keep Out Of Reach Of Children.

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

Other Information

store below 105°F.

Inactive Ingredients

Water (Aqua), Glycerin, Carbomer, Perfume (Fragrance), Aloe Barbadensis Leaf Extract, Aminomethyl Propanol.

* Please review the disclaimer below.