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Mckesson benzalkonium chloride towelette - Medication Information

Product NDC Code 68599-5807
Drug Name

Mckesson benzalkonium chloride towelette

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100g
Route TOPICAL
Dosage Form SWAB
RxCUI drug identifier 1038558
Application Number M003
Labeler Name McKesson Medical-Surgical
Packages
Package NDC Code Description
68599-5807-3 10 box in 1 case (68599-5807-3) / 100 packet in 1 box (68599-5807-2) / 1.5 g in 1 packet (68599-5807-1)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Benzalkonium Chloride, 0.13% w/v

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 Tear open packet Unfold and clean the affected area Discard after single use

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients water, sodium bicarbonate

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 Towelette to help prevent the risk of skin infection.

Purpose

Information about the drug product’s indications for use.
Purpose First Aid Antiseptic

Spl product data elements

Usually a list of ingredients in a drug product.
McKesson Benzalkonium Chloride Towelette Benzalkonium Chloride WATER SODIUM BICARBONATE 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.
Principal Display Panel - 0.13 g/100 g Case Label NDC 68599-5807-3 269 McKESSON Benzalkonium Chloride Towelettes ANTISEPTIC | GERMICIDAL | STERILE 100 PER BOX 10 BOXES PER CASE DO NOT REUSE Store at 59–86°F (15–30°C). Contents STERILE in unopened, undamaged inner package. Not made with natural rubber latex. Distributed By McKesson Medical-Surgical Inc. Richmond, VA 23233 Rev. 00 04/16 Made in China STERILE R MFR # 269 Principal Display Panel - 0.13 g/100 g Case Label Principal Display Panel - 0.13 g/100 g Box Label NDC 68599-5807-2 McKESSON Benzalkonium Chloride Towelettes ANTISEPTIC | GERMICIDAL | STERILE Helps prevent the risk of skin infection. 100 PER BOX DO NOT REUSE MFR # 269 Principal Display Panel - 0.13 g/100 g Box Label Principal Display Panel - 0.13 g/100 g Packet Label NDC 68599-5807-1 McKESSON Benzalkonium Chloride Towelettes ANTISEPTIC | GERMICIDAL | STERILE Helps prevent the risk of skin infection. Store at 59–86°F (15–30°C). Contents STERILE in unopened, undamaged package. Not made with natural rubber latex. DO NOT REUSE STERILE R MFR # 269 Principal Display Panel - 0.13 g/100 g Packet Label

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

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Consult a doctor in case of deep or puncture wounds, animal bites, or serious burns. Stop use and consult a doctor if the condition persists or gets worse.

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use longer than 1 week unless directed by a doctor.

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.
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 insert into the vagina. Do not use in the eyes or apply over large areas of the body. Consult a doctor in case of deep or puncture wounds, animal bites, or serious burns. Stop use and consult a doctor if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor. 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