Hand Sanitizer
FDA Label NDC 75613-006

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 75613-006). 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

  • Decrease bacteria and germs on the hands.
  • When water, soap and towel are not available
  • Recommended for repeated use

Warnings

For external use only.

Flammable.Keep away from fire and flame.

Do not apply around eyes.

Do not use in ears and mouth

When using this product

avoid contact with eyes. In case of contact, flush eyes with water.

Avoid contact with broken skin.

Stop use and ask a doctor if

irritation or redness develops or persists.

Keep Out Of Reach Of Children.

Children under 6, use only under adult supervision. Not recommended for infants.

Directions

  • pump as needed into your palms and thoroughly spread on both hands
  • rub into skin until dry

    • Other Information:

    • store at 20 ℃ (68 to 77℉)
    • may discolor fabrics

Inactive Ingredients

Glycerin,Propylene Glycol, Triethanolamine, Carbomer, Fragrance, Disodium Edta, Tocopheryl Acetate, Deionized Water

* Please review the disclaimer below.