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Product NDC Code | 21130-048 | ||||||
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Drug Name | Better living brands |
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Type | Brand | ||||||
Active Ingredients |
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Route | TOPICAL | ||||||
Dosage Form | SOAP | ||||||
RxCUI drug identifier | 1046593 | ||||||
Application Number | 505G(a)(3) | ||||||
Labeler Name | Better Living Brands LLC | ||||||
Packages |
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Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Benzalkonium chloride 0.13%
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.Directions Apply onto wet hands. lather and rinse thoroughly
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Water, Lauramidopropylamine oxide, Glycerin, Cetrimonium Chloride, Sodium chloride, Cocamide MEA , PEG-120 Methyl Glucose Dioleate, fragrance, Citric Acid , Tetrasodium EDTA, Sodium sulfate, Methylchloroisothiazolinone, Methylisothiazolinone, Red 40, Yellow 5, Red 33
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.helps eliminate bacteria on hands
Purpose
Information about the drug product’s indications for use.Antibacterial
Spl product data elements
Usually a list of ingredients in a drug product.Better Living Brands Benzalkonium Chloride EDETATE SODIUM WATER LAURAMIDOPROPYLAMINE OXIDE SODIUM CHLORIDE GLYCERIN SODIUM SULFATE METHYLCHLOROISOTHIAZOLINONE CETRIMONIUM CHLORIDE METHYLISOTHIAZOLINONE PEG-120 METHYL GLUCOSE DIOLEATE COCAMIDE CITRIC ACID ACETATE FD&C RED NO. 40 BASIC YELLOW 5 FRAGRANCE CLEAN ORC0600327 BENZALKONIUM CHLORIDE BENZALKONIUM
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.50 oz 11.25 oz
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.incase of accidental ingestion, seek medical attention or contact a poison control centre immediately.
Questions
A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.1-888-723-3929
Stop use
Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.Ask a doctor if irritation or redness develops and lasts
When using
Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Storage and handling
Information about safe storage and handling of the drug product.Store at room temperature
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.For external use only Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Ask a doctor if irritation or redness develops and lasts incase of accidental ingestion, seek medical attention or contact a poison control centre immediately.
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API