Otc - Active Ingredient
Active ingredients
Ethyl alcohol 70% V/V
Hand Sanitizer
FDA Label NDC 47993-310
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 47993-310). 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 hand sanitizing to reduce bacteria on the skin.
Warnings
Warnings:
Flammable. Keep away from fire or flame.For external use only.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - When Using
Keep away from eyes. Do not inhale or ingest.
Otc - Stop Use
Stop use and ask doctor if irritation or redness develops.
Dosage & Administration
Directions:
Squeeze small amount in your palm and briskly rub hands together, and allow to air dry. For children under 6, use with adult supervision. Not recommended for infants.
Other Safety Information
Other information:
Store below 110℉(43℃).May discolor certain fabrics or surface.
Inactive Ingredient
Inactive Ingredients:
Water,Glycerol,Aloe barbadensis leaf juice,Carbomer,Triethanolamine
Package Label.Principal Display Panel
Image Of Hand Sanitizer 29ml (29ml)
Image Of Hand Sanitizer 54ml (54ml)
Image Of Hand Sanitizer 237ml (237ml)
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