Otc - Active Ingredient
Active ingredients
Ethyl Alcohol 70%
Hand Sanitizer
FDA Label NDC 47993-228
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 47993-228). 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, warnings, indications & usage, otc - ask doctor, otc - stop use, dosage & administration, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiseptic
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.
Indications & Usage
Uses：
For hand sanitizing to readuce bacteria on the skin.
Otc - Ask Doctor
Stop use and ask a doctor if irritation or rash appears and lasts.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
Dosage & Administration
Directions:
Squeeze small amounnt in your palm and briskly rub hands together until dry.
Other Safety Information
Store below 110℉
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Inactive Ingredient
Inactive Ingredients:
Water,Carbomer ,Triethanolamine,Glycerin and Aloe Vera Extract
Package Label.Principal Display Panel
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