Hand Sanitizer Gel
FDA Label NDC 47993-363

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 Jiangbei Ocean Star Trading Co.,ltd for the product Hand Sanitizer (NDC 47993-363). 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, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredients

Ethyl Alcohol 62%

Otc - Purpose

Antiseptic

Indications & Usage

Uses：

For hand sanitizing to reduce bacteria on the skin.

Warnings

Warnings:

For external use only.

Flammable. Keep away from fire and flame.

Otc - When Using

When using this product，do not use in or near the eyes.In case of contact，rinse eyes thoroughly with water.

Otc - Stop Use

Discontinue use if irritation or redness develops.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.If swallowed，get medical help or contact a Poison Control Center right away.

Dosage & Administration

Directions:

Squeeze small amount in your palm and briskly rub hands together until dry.

Inactive Ingredient

Inactive Ingredients:

Water, Glycerin, Carbomer, Fragrance, Triethanolamine, Aloe Barbadensis Leaf Juice, Vitamin E, Iron Oxide（CI77499), Iron Oxide(CI 77492), D&C Red No.30.

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