Active Ingredient(S)
Ethyl Alcohol 75% v/v
Hand Sanitizer
FDA Label NDC 93782-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yangzhou Lianrun Medical Equipment Co., Ltd. for the product Hand Sanitizer (NDC 93782-002). 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 active ingredient(s), purpose, use, warnings, otc - stop use, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
- To decrease bacteris on the skin that potentially can cause disease
- Recommended for repeated use
Warnings
- Flammable, keep away from heat or flame
- For external use only
- Keep out of eyes, ears or mouth. In case of eye contact, flush eyes with water
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develop or if condition persists more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children swallowed, get medical help or contact a Poison Control Center right away. Children should be supervised by an adult when using this product.
Directions
Apply a small amount of product to your palm to cover both hands and rub until dry.
Other Information
- Store between 15-30°C(59-86°F)
- Avoid freezing and excessive heat above 40°C(104°F)
Inactive Ingredients
Aloe Vera Leaf, Alpha-Tocopherol Acetate, Carbomer Interpolymer Type A, Aloe(fragrance), Glycerin, Maltodextrin, Propylene Glycol, Water, Aminomethyl Propanol.
Package Label - Principal Display Panel
118 mL NDC: 93782-002-01
118ml Label (118)
500 mL NDC: 93782-002-02
500ml Label (500)
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