Otc - Active Ingredient
Active ingredients
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 47993-239
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 47993-239). 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 - keep out of reach of children, 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.
Label Section Quick Index
Otc - Purpose
Antiseptic
Indications & Usage
Uses：
For hand sanitizing to readuce bacteria on the skin.
Warnings
Warnings:
Flammable. Keep away from fire or flame. For external use only. Keep out of reach of children. Keep out of reach of eyes.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Dosage & Administration
Directions:
Place small amount in your palm and briskly rub hands together until dry.
Inactive Ingredient
Inactive Ingredients:
Water,Carbomer,Triethanolamine,Glycerin,Aloe Barbadensis Leaf Juice,Vitamin E
Package Label.Principal Display Panel
237ml (237ml)
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