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| Product NDC Code | 68599-5502 | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Drug Name | Antibacterial |
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| Type | Brand | ||||||||
| Active Ingredients |
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| Route | TOPICAL | ||||||||
| Dosage Form | LIQUID | ||||||||
| RxCUI drug identifier | 1039026 | ||||||||
| Application Number | M003 | ||||||||
| Labeler Name | McKesson | ||||||||
| Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient Benzethonium 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 • Apply to hands and wet as needed. • Lather vigorously for at least 15 seconds. • Wash skin, rinse thoroughly and dry.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients : Purified Water, Cocamidopropyl Betaine, Lauramine Oxide, Glycerin, Cetrimonium Chloride, Fragrance, DMDM Hydantoin, Iodopropynyl Carbamate, Yellow 5, Red 4, (may contain Citric Acid, Sodium Hydroxide)
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 handwashing to decrease bacteria on the skin.
Purpose
Information about the drug product’s indications for use.Purpose Antiseptic
Spl product data elements
Usually a list of ingredients in a drug product.Antibacterial Benzethonium Chloride LAURAMINE OXIDE CETRIMONIUM CHLORIDE DMDM HYDANTOIN IODOPROPYNYL BUTYLCARBAMATE WATER COCAMIDOPROPYL BETAINE GLYCERIN FD&C RED NO. 4 FD&C YELLOW NO. 5 BENZETHONIUM CHLORIDE BENZETHONIUM
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.NDC 68599-5502-1 McKesson Foaming Antibacterial Soap Clean Scent with Pump Net Contents 8.5 fl oz (251 mL) 53-23123-8.5
NDC 68599-5502-2 McKesson Foaming Antibacterial Soap Clean Scent Refill for McKesson Pump and Automatic Foam Dispensers MFR#s 53-FOAM and 53-Foam-Auto Net Contents 1000 mL (34 fl oz) 53-23126-1000 (2)
NDC 68599-5502-3 McKesson Foaming Antibacterial Soap Clean Scent with Pump Net Contents 18 fl oz (532 mL) 53-23127-18 (2)
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.Drug Facts
Other information - Protect from freezing. Avoid excessive heat.
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.
Questions
A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.General Questions? Call 1-800-777-4908
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. Do not use in the eyes. Discontinue use if irritation and redness develops. If condition persists for more than 72 hours consult a doctor.
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