Active Ingredient
Benzalkonium Chloride 0.13%
Hand Sanitizer
FDA Label NDC 76383-032
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bbc Group Limited for the product Hand Sanitizer (NDC 76383-032). 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 ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, 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
Uses
■ Hand sanitizing lotion to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only.
When Using This Product
■ keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes throughly with water.
Stop Use And Ask A Doctor If
irritation and redness develops and persists.
Keep Out Of Reach Of Children
If swallowed, contact a doctor or Poison Control Center right away.
Directions
■ Apply a dime-sized amount onto hands and rub together until absorbed. ■ Supervise children under 6 years of age when using this product
Inactive Ingredients
Water, Mineral Oil, Cetearyl Alcohol, Glycerin, Glyceryl Stearate, Steareth-25, PEG-100 Stearate, Urea, Dimethicone, Shea (Butyrospermum Parkii) Butter, Phenoxyethanol, Xanthan Gum, Lavender (Lavandula Angustifolia), Chlorphenesin, Sodium Hyaluronate
Package Label
Package Label (Bzklotn100mltbelavshealbl)
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