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| Product NDC Code | 0363-0242 | ||||||
|---|---|---|---|---|---|---|---|
| Drug Name | Walgreen |
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| Type | Brand | ||||||
| Active Ingredients |
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| Route | TOPICAL | ||||||
| Dosage Form | SOAP | ||||||
| RxCUI drug identifier | 1046593 | ||||||
| Application Number | part333E | ||||||
| Labeler Name | Walgreen | ||||||
| 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.-wet hands -apply palmful to hands -scrub thoroughly -rinse thoroughly
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Water (Aqua), Cetrimonium Chloride, Lauramidopropylamine Oxide, Glycerin, Lauramine oxide, Sodium Chloride, PEG-120 Methyl Glucose Dioleate, Citric Acid, Cocamide MEA, Fragrance (Parfum), Sodium Benzoate, Tetrasodium EDTA, Red 4 (Cl 14700), Yellow 5 (Cl 19140)
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.Hand washing
Purpose
Information about the drug product’s indications for use.Antibacterial
Spl product data elements
Usually a list of ingredients in a drug product.Walgreen Benzalkonium Chloride GLYCERIN PEG-120 METHYL GLUCOSE DIOLEATE COCO MONOETHANOLAMIDE FD&C RED NO. 4 LAURAMIDOPROPYLAMINE OXIDE FRAGRANCE CLEAN ORC0600327 WATER SODIUM CHLORIDE BENZALKONIUM CHLORIDE BENZALKONIUM CITRIC ACID MONOHYDRATE CETRIMONIUM CHLORIDE LAURAMINE OXIDE SODIUM BENZOATE FD&C YELLOW NO. 5 EDETATE SODIUM
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.333 mL
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.-Irritation and redness develops. -condition persists for more than 72 hours.
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 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.For External use only: Hands only Avoid contact with eyes. If contact occurs, rinse eyes with water. -Irritation and redness develops. -condition persists for more than 72 hours. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away.
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