Active Ingredient
Benzalkonium Chloride 0.066%
Pfa Stronghold Hand Sanitizer
FDA Label NDC 80969-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Stronghold Trading Llc for the product Pfa Stronghold Hand Sanitizer (NDC 80969-001). 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, use, warnings, otc - when using, 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
Disinfectant
Use
Hand sanitizing to help reduce bacteria on the skin.
Warnings
For external use only.
Flammable. Keep away from fire or flame.
Otc - When Using
When using this product, avoid contact with the eyes.
In case of contact, flush eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develops and persists.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
- Put enough product in the palm to cover hands & rub together briskly the liquid is dry.
- Children under 6 should be supervised when using Sanitizers.
Other Information
- Store below 110°F (43°C)
- May discolor certain fabrics or surfaces.
Inactive Ingredients
Water, Glycerin, Carbomer, Triethanolamine, Mentha Piperita (Peppermint) Oil, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Morus Alba Bark Extract, Panthenol
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