Otc - Active Ingredient
Active ingredients
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 47993-364
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 47993-364). 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 - 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:
Put enough product in your palm to cover hands and rub hands together briskly until dry.
Children under 6 years of age should be supervised when using this product.
Other Safety Information
Other information
Store Below 110℉（43℃）
May discolor certain fabrocs or surfaces
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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