Otc - Active Ingredient
Active ingredients
Ethyl Alcohol 62%(V/V)
Hand Sanitizer
FDA Label NDC 47993-289
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 47993-289). 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 decrease bacteria on the skin.
Warnings
Warnings：
For external use only-hands
Flammable.
Keep away from heat or flame.
Otc - When Using
When using this product
- avoid contact with eyes. In case of contact flush eyes thoroughly with water.
Otc - Stop Use
Stop and ask doctor if
skin irritation or redness develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
If swallowed, get medical help or contact Poison Control Center right away.
Dosage & Administration
Directions:
- Wet hands thoroughly with product and allow to dry without wiping.
- Children under 6 years of age should be supervised when using this product.
Other Safety Information
Other information:
- Do not store above 104℉ (40℃).
- May discolor certain fabrics or surfaces.
Inactive Ingredient
Inactive Ingredients:
Water (Aqua),Glycerin,Aloe Barbadensis Leaf Juice,Carbomer,Triethanolamine,Fragrance
Package Label.Principal Display Panel
Image Of Hand Sanitizer 30ml (30ml)
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