Antibacterial Hand Sanitizer Gel
FDA Label NDC 73796-111

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Prostock Llc for the product Antibacterial Hand Sanitizer (NDC 73796-111). 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 ingredients, purpose, uses, warnings, other, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

For hand washing to decrease bacteria on the skin.

Warnings

For external use only.

Other

Flammable.  Keep away from heat and 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

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 a product and allow to dry without wiping.

Other Information

Store under 105 o F. 

Inactive Ingredients

Water, Polyquaternium-10, Propylene Glycol, Glycerin, Polyaminopropyl Biguanide, PEG-40 Hydrogenated Castor Oil, Fragrance, Tromethamine

Package Labeling:

73796-111-20 (73796 111 20)

73796-111-20 (73796 111 20)

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