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| Product NDC Code | 20276-138 | ||||
|---|---|---|---|---|---|
| Drug Name | Lucky super soft foaming |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | SOAP | ||||
| RxCUI drug identifier | 1046593 | ||||
| Application Number | part333A | ||||
| Labeler Name | Delta Brands, Inc | ||||
| 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 ■ wet hands and apply soap ■ lather all surfaces of hands and fingers by rubbing vigorously for at least 20 seconds ■ rinse hands well and dry
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients water, glycerin, lauramine oxide, cetrimonium chloride, cocamidopropyl betaine, decyl glucoside, hydroxypropyl methylcellulose, fragrance, zinc sulfate, citric acid, sodium chloride, tetrasodium EDTA, alcohol, methylchloroisothiazolinone, methylisothiazolinone
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.Use 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.LUCKY SUPER SOFT FOAMING Benzalkonium chloride WATER DECYL GLUCOSIDE LAURAMINE OXIDE GLYCERIN CETRIMONIUM CHLORIDE COCAMIDOPROPYL BETAINE HYPROMELLOSE, UNSPECIFIED ZINC SULFATE METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE EDETATE SODIUM CITRIC ACID MONOHYDRATE SODIUM CHLORIDE ALCOHOL 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.Package Label package label
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 If swallowed, get medical help or contact a Poison Control Center right away.
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 use and ask a doctor if irritation and redness develops
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.When using this product avoid contact with the eyes. In case of eye contact, flush with water.
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.Warnings 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