Otc - Active Ingredient
Active ingredients
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 47993-226
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 47993-226). 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, otc - when using, otc - stop use, otc - keep out of reach of children, indications & usage, 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
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. In case of contact with eyes，flush thoroughly with water. Avoid contact with broken skin. 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
If swallowed，get medical help or call a Poison Control Center right away.
Indications & Usage
Uses：
For hand sanitizing.
Dosage & Administration
Directions:
Wet hands thoroughly with product and allow to dry without wiping.
For children under 6,use only under adult supervision.
Not recommended for infants.
Other Safety Information
Do not store above 105℉.
May discolor some fabrics.
Inactive Ingredient
Inactive Ingredients:
Water,Carbomer 940,Triethanolamine,Glycerin,Aloe barbadensis leaf juice
Package Label.Principal Display Panel
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