Otc - Active Ingredient
Alkyl Dimethyl Benzyl Ammonium Chloride 0.5%
Gel
FDA Label NDC 75594-190
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Commercial Beverage Concepts Llc for the product Gel (NDC 75594-190). 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, indications & usage, inactive ingredient, otc - keep out of reach of children, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
For hand-washing to decrease bacteria on the skin. Rocommended for repeated use.
Warnings
- For external use only: hands
- Do not use if you are allergic to any of the ingedients listed below
- avoid contact with eyes. In case of eye contact, flush thoroughly with water
- irritation and redness develop
When using this product:
Stop use and ask a doctor if:
Indications & Usage
Directions:
- Wet hands
- Rinse well and dry hands completely
Inactive Ingredient
Water, Sodium Olefin Sulfonate, Lauramine Oxide, Dimethyletradecylamine Oxide, Sodium Sulfonate, Cocamide DEA, Glycerin, Diethanolamine, Citric Acid, Fragrance, Dye
Otc - 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
Dosage & Administration
Apply small amount of product and work into a lather
* Please review the disclaimer below.
