Otc - Active Ingredient
Active ingredients
Alcohol 70% v/v
Hand Sanitizer
FDA Label NDC 47993-256
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 47993-256). 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：
Hand sanitizer to help reduce bacteria on the skin that could cause disease.
Warnings
Warnings:
For external use only
Flammable. Keep away from fire or flame.
Otc - When Using
When using this product.
Do not get into eyes. If contact occurs，rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor.
If irritation or rash appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
If swallowed，get medical help or contact a Poison Control Center right away.
Dosage & Administration
Directions:
- Place enough product in your palm
- Rub hands vigorously until dry
- Children under 6 years of age should be supervised when using this product
Other Safety Information
Other information
- Store below 106℉（41℃）
- May discolor certain fabrics or surfaces
Inactive Ingredient
Inactive Ingredients:
Water,Carbomer,Triethanolamine,Glycerin,Aloe Barbadensis Leaf Extract
Package Label.Principal Display Panel
100ml (100ml)
237ml (237ml)
500ml (500ml)
1000ml (1000ml)
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