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PROBALANCE Hand Sanitizer Advanced Gel
Drug Facts
Probalance Hand Sanitizer Advanced
FDA Label NDC 78072-501
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ltd Enterprises Distribution, Inc. for the product Probalance Hand Sanitizer Advanced (NDC 78072-501). 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 other, purpose, use, warnings, when using this product, otc - stop use, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Hand Sanitizer to help reduce bacteria on the skin.
Warnings
Flammable. Keep away from source of heat, fire or flame.
For external use only. Not for Consumption.
When Using This Product
When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops and lasts.
Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions
- place enough product in your palm to thoroughly cover your hands and rub hands together until dry.
- children under 6 years should be supervised when using this product.
Inactive Ingredients
Water, hydroxypropyl guar, citric acid
Active Ingredient
Alcohol 70% v/v
Other Information
Other information
- store at a temperature below 110 F (43 C).
- may discolor certain fabrics or surfaces.
Package Label - Principal Display Panel
Label (Probalance 8oz 20may20)
78072-501-10 - 1 gallon
One Gallon Label (Probalance 1gal 20may20)
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