Otc - Active Ingredient
Active ingredients
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 47993-227
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 47993-227). 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, warnings, otc - do not use, otc - stop use, otc - ask doctor, indications & usage, 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
Warnings
Warnings:
Do not use in the eyes. In case of contact，rinse eyes with water. Stop use and ask a doctor if irritation and redness develop and last for more than 72 hours. Get medical help immediately if swallowed. Flammable，keep away from fire or flame. For external use only.
Otc - Do Not Use
Do not use in the eyes. In case of contact，rinse eyes with water.
Otc - Stop Use
if irritation and redness develop and last for more than 72 hours.
Otc - Ask Doctor
if irritation and redness develop and last for more than 72 hours.
Indications & Usage
Uses：
Hand sanitizer to decrease bacteria on the skin
Dosage & Administration
Diections：
Apply small amount and rub hands together until dry.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Inactive Ingredient
Inactive Ingredients:
Water,Carbomer,Triethanolamine,Glycerin and Aloe VeraExtract
Package Label.Principal Display Panel
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