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| Product NDC Code | 51316-703 | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Drug Name | Handsoap |
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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 | CVS Pharmacy | ||||||||
| 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.
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.Apply onto dry hands. Work into a lather, rinse and dry throughly.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.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 (Cl16035), Yellow 5 (Cl 19140), Red 33 (Cl 17200)
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 skin
Purpose
Information about the drug product’s indications for use.Purpose Antibacterial
Spl product data elements
Usually a list of ingredients in a drug product.Handsoap Benzalkonium Chloride GLYCERIN COCO MONOETHANOLAMIDE PEG-120 METHYL GLUCOSE DIOLEATE CITRIC ACID MONOHYDRATE FD&C RED NO. 40 BASIC YELLOW 5 EDETATE SODIUM D&C RED NO. 33 WATER CETRIMONIUM CHLORIDE SODIUM CHLORIDE LAURAMIDOPROPYLAMINE OXIDE SODIUM SULFATE METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE 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.56 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.In case of accidental ingestion, seek medical attention or contact a poison control centre immediately
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
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 In case of accidental ingestion, seek medical attention or contact a poison control centre immediately ask a doctor if Irritation or redness develops and lasts
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