Active Ingredient
Benzalkonium Chloride 0.13%
Berkley Jenson Antibacterial Hand
FDA Label NDC 68391-151
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 Jenson Antibacterial Hand (NDC 68391-151). 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
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 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, get medical help or contact a Poison Control Center immediately.
Directions
appy onto wet hands. Lather and rinse thoroughly
Other Information
store at room temperature.
Inactive Ingredients
Water (Aqua), Cocamidopropyl Betaine, Glycerin, Decyl Glucoside, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Poloxamer 124, Polyquaternium-7, Tetrasodium EDTA, Citric Acid, Sodium Citrate, Camellia Sinensis Leaf Extract, Saccharomyces Ferment, Tocopheryl Acetate, Retinyl Palmitate, Ascorbyl Palmitate, Niacinamide, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200).
Questions Or Comments?
1-800-934-1204
Label Copy
Image Of The Label (20118l)
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