Otc - Active Ingredient
Active ingredients
Ethyl Alcohol 68%
Hand Sanitizer
FDA Label NDC 47993-222
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 47993-222). 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 - ask doctor, otc - stop use, indications & usage, dosage & administration, otc - keep out of reach of children, 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 - Ask Doctor
In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately
Otc - Stop Use
Stop use and ask a doctor if skin irritation develops.
Indications & Usage
Uses：
To decrease bacteria and germs on the skin.
Recommended for repeated use.
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.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. For children under 6,use only under adult supervision.
Other Safety Information
Do not store above 105℉
May discolor some fabrics
Harmful to wood finishes and plastics
Inactive Ingredient
Do not store above 105℉
May discolor some fabrics
Harmful to wood finishes and plastics
Package Label.Principal Display Panel
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