Active Ingredients
Benzalkonium Chloride 0.13%
Fresh Water Antibacterial Foaming Hand
FDA Label NDC 63148-110
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Apollo Health And Beauty Care Inc. for the product Fresh Water Antibacterial Foaming Hand (NDC 63148-110). 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 ingredients, 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
For hand washing to decrease bacteria on the skin.
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 for more than 72 hours.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
- Apply onto dry hands.
- Lather and rinse thoroughly with water.
Other Information
Store at room termpature
Inactive Ingredients
Water (Aqua), Cocamdiopropyl Betaine, Polysorbate 20, Fragrance (Parfum), Glycerin, Decyl Glucoside, Aloe Barbadensis Leaf Juice, Camellia Sinensis Leaf Extract, Polyquaternium-7, Xanthan Gum, Propylene Glycol, Tetrasodium EDTA, Sodium Citrate, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Ext. Violet 2 (CI 60730).
Label Copy
Image Of The Label (21651l)
* Please review the disclaimer below.
