Otc - Active Ingredient
Active Ingredients
Ethyl alcohol 70%
Hand Sanitizer
FDA Label NDC 47993-321
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 47993-321). 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-hands.Flammable.Keep away from heat and flame.
Otc - When Using
when using this product: Keep out of eyes. Do not inhale or ingest.
Otc - Stop Use
Stop use and ask a doctor if Skin irritation develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Dosage & Administration
Directions:
Squeeze small amount in your palm and briskly rub hands together until dry.
Inactive Ingredient
Inactive Ingredients:
Water, Glycerin, Carbomer, Aloe Barbadensis leaf juice, Aminomethyl Propanol.
Package Label.Principal Display Panel
Image Of Hand Sanitizer 30ml (30ml)
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