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| Product NDC Code | 36800-535 | ||||
|---|---|---|---|---|---|
| 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 | Topco Associates 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
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.Dosage Section Topical use only. Use when required.
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 (CI 16035), Yellow 5 (CI 19140), Red 33 (CI 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.Directions . Use only to refill a Liquid Hand Soap pump bottle. . From pump bottle, apply onto wet hands. . Lather and rinse thoroughly.
Purpose
Information about the drug product’s indications for use.Handwashing
Spl product data elements
Usually a list of ingredients in a drug product.Handsoap Benzalkonium chloride CITRIC ACID MONOHYDRATE EDETATE SODIUM METHYLISOTHIAZOLINONE GLYCERIN WATER FD&C RED NO. 40 LAURAMIDOPROPYLAMINE OXIDE CETRIMONIUM CHLORIDE SODIUM CHLORIDE COCO MONOETHANOLAMIDE PEG-120 METHYL GLUCOSE DIOLEATE METHYLCHLOROISOTHIAZOLINONE FD&C YELLOW NO. 5 D&C RED NO. 33 SODIUM SULFATE 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
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, get medical help or contact a Poison Control Center 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.Stop using this product and 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. In case of contact, flush 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
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