Active Ingredient.
Benzalkonium Chloride (0.13%)
Giant Eagle Soap
FDA Label NDC 56194-502
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Giant Eagle for the product Giant Eagle (NDC 56194-502). 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 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, get medical help or contact a Poison Control Center immediately.
Directions
- Apply onto wet 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, Polyquaternium-7, Tetrasodium EDTA, Sodium Citrate, Citric Acid, Benzophenone-4, Methylchloroisothiazolinone, Methylisothiazolinone, Ext. Violet 2 (CI 60730).
Principal Display Panel
Pdp-01 (Pdp 01)
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