Active Ingredients:
Alcohol 62%
Pure Vitac Instant Hand Sanitizer
FDA Label NDC 53152-0001
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 Pure Vitac Instant Hand Sanitizer (NDC 53152-0001). 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 ingredients:, purpose, use, warning:, when using this product, ask a doctor before use if you have, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
To help reduce bacteria on the hands that can potentially cause disease.
Warning:
- For External Use Only
- Flammable, Keep away from fire or flame
When Using This Product
- Avoid contact with eyes, if this occurs rinse thoroughly with water and contact a physician
Ask A Doctor Before Use If You Have
- Deep wounds, animal bites or serious burns.
Stop Use And Ask A Doctor If
- significant irritation or sensitization occurs
Keep Out Of Reach Of Children
- If swallowed get medical help or contact a Poison Control Center immediately
Directions:
Apply a liberal amount to hands and rub hands thoroughly until dry. Do not rinse or wipe off gel.
Inactive Ingredients:
Deionized water, Aloe Barbadenis Leaf Juice, Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol, Fragrance
Package Label.Principal Display Panel
Image Of Bottle Label (A1oz)
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