Antibacterial Hand Sanitizer Gel
FDA Label NDC 73145-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Asc Marketing Ltd for the product Antibacterial Hand Sanitizer (NDC 73145-004). 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 drug facts, active ingredient, purpose, uses, warnings, when using this product, keep out of reach of children., if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

  • for handwashing to decrease bacteria on the skin. 
  • recommended for repeated use.

Warnings

For external use only.

When Using This Product

• Do not use in eyes.
• Discontinue use if irritation and redness develop.

Flammable, keep away from fire or flame.

Keep Out Of Reach Of Children.

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

If Pregnant Or Breast-Feeding,

ask a health professional before use.

Directions

• wet hands thoroughly with product.
• briskly rub hands together until dry.

Inactive Ingredients

Deionized Water, Glycerin, Propylene Glycol, Triethanolamine, Carbomer, Methylparaben, Proplyparaben, Fragrance

Package Labeling:

Label (Label)

Label (Label)

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