Active Ingredient.
Benzalkonium Chloride (0.13%)
Careone Amber Soap
FDA Label NDC 72476-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Retail Business Services, Llc for the product Careone Amber (NDC 72476-004). 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., 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 Poison Control Center immediately.
Directions
- apply onto wet hands (only for 222 ml and 333 ml)
- Lather and rinse thoroughly.(For all packages)
- From a pump bottle, apply onto wet hands (only for 1.66 L bottle)
- Use to refill a pump bottle (only for 1.66 L bottle)
Other Information
Store at Room Temperature
Inactive Ingredients
Water (Aqua), Lauramidopropylamine Oxide, Glycerin, Cetrimonium Chloride, Sodium Chloride, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Fragrance (Parfum), Citric Acid, Tetrasodium EDTA, Sodium Sulfate, Methylchloroisothiazolinone, Methylisothiazolinone, Red 40 (Cl 16035), Yellow 5 (Cl 19140), Red 33 (Cl 17200).
Questions Or Comments?
1-877-846-9949
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