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Pacific blue ultra antimicrobial foam pacific citrus - Medication Information

Product NDC Code 54622-317
Drug Name

Pacific blue ultra antimicrobial foam pacific citrus

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100ml
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 1046593
Application Number 505G(a)(3)
Labeler Name Georgia-Pacific Consumer Products
Packages
Package NDC Code Description
54622-317-01 4 bottle in 1 box (54622-317-01) / 1200 ml in 1 bottle
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Active ingredient

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

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, apply soap, rub hands together vigorously for at least 20 seconds. Rinse and dry hands thoroughly with a disposable paper towel.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Water (Aqua), Lauramine Oxide, Lauryl Betaine, Laurtrimonium Chloride, Glycerin, Sodium PCA, Tocopheryl Acetate, Oleth-10, Tetrasodium EDTA, Citric Acid, Fragrance, FD&C Yellow #6, FD&C Red #40

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 Handwash to help reduce bacteria that potentially can cause disease.

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.
Pacific Blue ultra Antimicrobial Foam Pacific Citrus Benzalkonium Chloride FD&C RED NO. 40 WATER BENZALKONIUM CHLORIDE BENZALKONIUM .ALPHA.-TOCOPHEROL, DL- EDETATE SODIUM SODIUM PIDOLATE OLETH-10 FD&C YELLOW NO. 6 GLYCERIN LAURTRIMONIUM CHLORIDE ANHYDROUS CITRIC ACID LAURYL BETAINE LAURAMINE OXIDE

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.
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

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, seek immediate medical attention or call a poison control center.

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 if irritation or redness develops. If condition persists for more than 72 hours consult a doctor.

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 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 When using this product Avoid contact with eyes. In case of eye contact, flush with water. Stop use if irritation or redness develops. If condition persists for more than 72 hours consult a doctor. Keep out of reach of children. If swallowed, seek immediate medical attention or call a poison control center.

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