Drug Facts - Active Ingredient
Benzalkonium Chloride 0.09%
Antibacterial Sanitizing And Moisturizing Hand
FDA Label NDC 83388-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Qblue Technologies, Inc. for the product Antibacterial Sanitizing And Moisturizing Hand (NDC 83388-003). 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 drug facts - active ingredient, purpose, uses, warnings, avoid contact with eyes., do not use, if irritation develops, 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
Uses
Hand sanitizer to help reduce bacteria that potentially can cause disease.
Warnings
For external use only
Avoid Contact With Eyes.
In case of contact, rinse eyes thoroughly with water.
Do Not Use
on open skin wounds.
If Irritation Develops
Discontinue use and consult a doctor.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact poison control center right away.
Directions
Apply product thoroughly to hands.
Rub hands together until absorbed.
Do not wipe off or rinse. Apply to
hands as needed.
Other Information
Avoid direct sunlight. Store below
50°C. Do not refrigerate.
Inactive Ingredients
Purified Water, Mineral Oil, Glyceryl
Stearate, Stearic Acid, Fragrance,
Cetearyl Alcohol, Acrylates /C10-30
Alkyl Acrylate, Glycerin, Sodium
Hydroxide, Crosspolymer, Vitamin B,
Vitamin E, Titanium Dioxide.
Questions Or Comment?
1-833-387-9949
Pdp
NDC: 83388-001-15
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