Otc - Active Ingredient
Active Ingredients
Ethyl alcohol 62%
Hand Sanitizer
FDA Label NDC 47993-320
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 47993-320). 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 - keep out of reach of children, otc - when using, otc - stop use, 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：
For sanitizing hands to reduce bacteria and viruses on the skin.
Warnings
Warnings:
Flammable. Keep away from fire and flame.
For external use only.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children or pets.
Otc - When Using
Do not put in eyes.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
Dosage & Administration
Directions:
Apply small amount in your palm and briskly rub hands together until dry.
Inactive Ingredient
Inactive Ingredients:
Water, Glycerin, Carbomer, Fragrance, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Vitamin E, Iron Oxide(CI 77499),
Iron Oxide(CI 77492), D&C Red No.30.
Package Label.Principal Display Panel
Image Of Hand Sanitizer 1000ml-2 (1000ml 2)
Image Of Hand Sanitizer 5000ml-1 (5000ml 1)
Image Of Hand Sanitizer 1000ml-1 (1000ml 1)
Image Of Hand Sanitizer 5000ml-2 (5000ml 2)
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