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| Product NDC Code | 52000-043 | ||||
|---|---|---|---|---|---|
| Drug Name | Antibacterial handwash tropical beach |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | LIQUID | ||||
| RxCUI drug identifier | 1046593 | ||||
| Application Number | part333E | ||||
| Labeler Name | Universal Distribution Center 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.Active Ingredient 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 Pump a small amount of soap into wet hands, rub hands together to create rich lather, then rinse.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Ingredients: Water, Sodium Laureth Sulfate, Sodium Chloride, Cocamidopropyl Betaine, Cocamide MIPA, Laureth-4, Glycerin*, Polyquaternium-7*, Fragrance, Methylchloroisothiazolinone, Methylisothiazolinone, Tetrasodium EDTA, Citric Acid, Benzophenono-4, Tocopheryl Acetate, FD&C Blue No. 1, D&C Red No. 33 *Contains one or more of these ingredients.
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.USES for hand washing to decrease bacteria on the 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.ANTIBACTERIAL HANDWASH TROPICAL BEACH benzalkonium chloride BENZALKONIUM CHLORIDE BENZALKONIUM WATER SODIUM LAURETH-3 SULFATE SODIUM CHLORIDE COCAMIDOPROPYL BETAINE COCO MONOISOPROPANOLAMIDE LAURETH-4 GLYCERIN POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE EDETATE SODIUM CITRIC ACID MONOHYDRATE SULISOBENZONE .ALPHA.-TOCOPHEROL ACETATE FD&C BLUE NO. 1 D&C RED NO. 33
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.Packaging Tropical1
Spl unclassified section
Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.Kill Germs and Odors Distributed By: Universal Distribution Center 96 Distribution Boulevard, Edison, NJ 08817 Made in Turkey
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.Keep out of reach of children.
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.Warning: Avoid contact with eyes. In case of contact flush with water. Keep out of direct sunlight. Do not drink, not edible. External use only. Keep out of reach of children.
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