Otc - Active Ingredient
Active ingredients
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 47993-261
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 47993-261). 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, inactive ingredient, indications & usage, dosage & administration, warnings, otc - keep out of reach of children, otc - purpose, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Inactive Ingredients:
Water,Carbomer,Triethanolamine,Glycerol and Aloe Vera Extract.
Indications & Usage
Uses：
Hand sanitizer to decrease bacteria on the skin.
Dosage & Administration
Apply small amount and rub hands together until dry.
Warnings
Warnings:
Do not use in the eyes. In case of contact, rise 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 - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Purpose
Antiseptic
Package Label.Principal Display Panel
237ml (237ml)
500ml (500ml)
* Please review the disclaimer below.
