Otc - Active Ingredient
Active Ingredients:
Ethyl Alcohol 62%
Instant Hand Sanitizer
FDA Label NDC 53152-2002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aoss Medical Supply, Inc. for the product Instant Hand Sanitizer (NDC 53152-2002). 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 - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antiseptic
Warnings
Warning
For External Use Only.
Flammable, Keep away from fire or flame.
Otc - Stop Use
Stop use and ask a doctor if
significant irritation or sensitization occurs.
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
DIRECTIONS:
Apply a liberal amount to hands and rub hands thoroughly until dry. Do not rinse or wipe off gel.
Inactive Ingredient
INACTIVE INGREDIENTS:
Deionized water, Aloe barbadenis, Leaf Juice, Glycerin,
Propylene glycol, Carbomer, Aminomethyl Propanol, Fragrance
Otc - Ask Doctor
Ask a doctor before use if you have
Deep wounds, animal bites or serious burns.
Indications & Usage
Uses
To help reduce bacteria on the hands that can potentially cause disease.
Otc - When Using
When using this product
Avoid contact with eyes, if this occurs rinse thoroughly with water and contact a physician.
Package Label.Principal Display Panel
Image Of Bottle Label (118ml)
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