Hand Sanitizer
FDA Label NDC 75613-009

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Lanzi Cosmetic Technology Co., Ltd for the product Hand Sanitizer (NDC 75613-009). 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, use, warnings, keep out of reach of children., directions, inactive ingredients, packaging, 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

Use

Helps reduce bacteria on skin.

Warnings

For external use only

Flammable. Keep away from fire.

When using this product

Do not use on damaged or broken skin. keep out of eyes. In case of eye contact, immediately flush eyes with water then contact physician.

Stop use and ask a doctor if rah occurs.

Other Information:

  • Do not store above 110℉

Keep Out Of Reach Of Children.

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

Directions

  • Wet hands thoroughly with product and rub hands together briskly until dry.

Inactive Ingredients

Glycerin, Propylene Glycol, Triethanolamine, Carbomer, Fragrance, Disodium edta, Tocopheryl acetate, Deionized Water

* Please review the disclaimer below.