Otc - Active Ingredient
Active ingredients
Ethanol Alcohol 71% v/v
Hand Sanitizer
FDA Label NDC 47993-330
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 47993-330). 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, inactive ingredient, 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 germs on the skin.
Warnings
Warnings:
Flammable. Keep away from fire or flame.
For external use only.
Otc - When Using
When using this product, do not use in or near the eyes. In case of contact, rinse 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 and pets.
If swallowed, get medical help or contact a Poison Control Center Immediately.
Inactive Ingredient
Inactive Ingredients
Water,Glycerin,Propylene Glycol,Fragrance,Aloe Barbadensis Leaf Juice,Tocopherol Acetate(VITAMIN E)
Other Safety Information
Other information
Store below 106℉(41℃)
May discolor certain fabrics or surfaces
Dosage & Administration
Directions
Spray product into palms and rub together until dry.
Adult supervision is recommended for children under age 6.
Package Label.Principal Display Panel
Image Of Hand Sanitizer 29.87ml (29.87ml)
Image Of Papercard1 (Papercard1)
Image Of Papercard2 (Papercard2)
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