Aurafresh Instant Hand Sanitizer With Aloe And Vitamin E
FDA Label NDC 40104-287

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 Pulisi Daily Chemical Products Co., Ltd. for the product Aurafresh Instant Hand Sanitizer With Aloe And Vitamin E (NDC 40104-287). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active ingredient                                  Purpose

Ethyl Alcohol                62%      ...        Antiseptic

Otc - Purpose

Hand sanitizer to help decrease bacteria on the skin.

Otc - Keep Out Of Reach Of Children

If swallowed, get medical help or contact local poison control center right away.

Children under 6 years of age should be supervised by an adult when using.

Indications & Usage

when using this product, avoid contact with face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Warnings

For external use only.
Flammable. Keep away from hear or flame.

Stop using and ask a doctor, if irritation and redness develops.

Dosage & Administration

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

Inactive Ingredient

Water, Carbomer, Glycerin, Propylene Glycol, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Fragrance

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