Hand Sanitizer
FDA Label NDC 75613-020

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 75613-020). 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

For hand sanitizing

Warnings

For external use only.

Flammable. Keep product away from heat or flame.

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.

Do not inhale or ingest.

Stop use and ask a doctor if skin irritation develops.

Keep Out Of Reach Of Children.

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

Directions

  • Wet hands thoroughly with product and allow to dry without wiping.
  • For children under 6 age use only under adult supervision.
  • Not recommended for infants.

Inactive Ingredients

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

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