Antiseptic Hand Sanitizer Gel
FDA Label NDC 76138-113

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Innovation Specialties Inc for the product Antiseptic Hand Sanitizer (NDC 76138-113). 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 ingredients, purpose, use, warnings, directions, inactive ingredients, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredients

Ethyl Alcohol 62%

Purpose

Antiseptic

Use

To help clean hands

Warnings

For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes.

When using this product, avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if redness or irritation develop & persist for more than 72 hrs.

Directions

• Spread on both hands.

Inactive Ingredients

Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water.

Other Information

• store at 20°C (68° to 77° F). • may discolor fabrics.

Questions

Call 1-855-755-5346

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