Hand Sanitizer
FDA Label NDC 74649-003

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Yiwu Pharmacy Ecomm Business Enterprise Ltd for the product Hand Sanitizer (NDC 74649-003). 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 if, 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 70% v/v   

Purpose

Antibacterial

Uses

  • hand sanitizer to help reduce bacteria on the skin that may cause disease.

Warnings

For external use only. Store below 110°F(43°C)

Flammable. Keep away from heat or flame.

When Using This Product

  • avoid contact with face, eyes and broken skin. If eye contact occurs flush thoroughly with water.

Stop Use And Ask A Doctor If

  • irritation and redness develop and persist for more than 72 hours.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact Poison Control Center right away. Not recommended for infants.

Directions:

wet hands thoroughly with product and rub into skin until dry.

  • For children under 6, use under adult supervision.

Other Information:

May discolor some fabrics, Harmful to wood finishes and plastics.

Inactive Ingredients:

water, aloe barbadensis leaf juice, carbomer, propylene glycol, peg-12 dimethicone, triethanolamine.

Package Labeling:

Label (Label)

Label (Label)

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