Active Ingredient
Benzalkonium Chloride 0.13%
Berkley Jensen Foaming Hand
FDA Label NDC 68391-105
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bjwc for the product Berkley Jensen Foaming Hand (NDC 68391-105). 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., directons, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Uses
helps eliminate bacteria on hands.
Warnings
For external use only.
When Using This Product
avoid contact with eyes. In case of contact, rinse thoroughly with water.
Stop Use And Ask A Doctor If
irritation or redness develops and lasts.
Keep Out Of Reach Of Children.
In case of accidental ingestion, seek medical attention or contact a poison control center immediately.
Directons
Apply onto hands, lather and rinse thoroughly.
Other Information
store at room temperature.
Inactive Ingredients
Water (Aqua), Cocamidopropyl Betaine, Polysorbate 20, Fragrance (Parfum), Glycerin, Decyl Glucoside, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Camellia Sinensis Leaf Extract, Propylene Glycol, Polyquaternium-7, Tetrasodium EDTA, Sodium Citrate, Citric Acid, Benzophenone-4, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Ext. Violet 2 (CI 60730).
Label Copy
Image Of The Label (21580l)
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