Otc - Active Ingredient
Active Ingredients
Ethyl alcohol 75% v/v
Hand Sanitizer
FDA Label NDC 47993-319
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 47993-319). 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：
Hand sanitizer to help reduce bactria on the skin.
Warnings
Warnings:
Flammable. Keep away from fire and flame.
For external use only.
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
Stop use and ask a doctor if irritation or rash appears and lasts.
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 fabrics or surface.
Inactive Ingredient
Inactive Ingredients:
Water, Glycerin, Carbomer, Fragrance, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Vitamin E.
Package Label.Principal Display Panel
Image Of Hand Sanitizer 60ml (60ml)
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