Otc - Active Ingredient
Ethyl Alcohol 70%
Hand Cleansing Gel
FDA Label NDC 76701-700
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hand Sanitizer Llc for the product Hand Cleansing Gel (NDC 76701-700). 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 - stop use, otc - keep out of reach of children, dosage & administration, other safety information, 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
Hand Cleanser to help reduce bacteria on the skin.
Warnings
Flammable, Keep away from fire or flame.
For External use only
When using this product do not use in or near the eys. In case of contact, rinse eyes intensely with water.
Otc - Stop Use
Stop Use and ask a doctor if irritation or rash occurs and remains.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center immediately.
Dosage & Administration
Put enough product in your palm to cover hands well and rub hands together until dry. Children under 6 years old should be supervised when using.
Other Safety Information
Store under 110°F (43°C)
Inactive Ingredient
Water (Aqua), Hydroxypropyl Cellulose, Glycerin, Fragrance
Package Label.Principal Display Panel
70% Alcohol Cleansing Gel
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