Otc - Active Ingredient
Active ingredients
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 47993-211
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 47993-211). 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, recent major changes, warnings, otc - stop use, dosage & administration, otc - keep out of reach of children, 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.
Recent Major Changes
Uses:
For hand sanitizing to reduce bacteria on the skin.
Directions:
Squeeze small amount in your palm and briskly rub hands together, and allow to air dry.
Warnings
Warnings:
Flammable. Keep away from fire or flame. For external use only. 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.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Other Safety Information
Other Information
Store below 110F(43C). May discolor certain fabrics or surfaces.
Inactive Ingredient
Inactive ingredients
Water，Carbomer 940，Triethanolamine，Glycerin，Aloe Barbadensis
Package Label.Principal Display Panel
75ml (75ml)
237ml (237ml)
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