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| Product NDC Code | 54622-146 | ||||
|---|---|---|---|---|---|
| Drug Name | Enmotion foam |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | SOLUTION | ||||
| RxCUI drug identifier | 1038799 | ||||
| Application Number | 505G(a)(3) | ||||
| Labeler Name | Georgia Pacific Consumer Products | ||||
| 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 0.1%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 thoroughly with product and allow to dry without wiping.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Water, Decyl Glycoside, PEG-12 Dimethicone, Glycerin, Dipotassium Phosphate, Potassium Phosphate
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 To decrease bacteria on skin that could cause disease Recommended for repeated use
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.enMotion Foam Benzalkonium chloride WATER DECYL GLUCOSIDE PEG-12 DIMETHICONE GLYCERIN DIBASIC POTASSIUM PHOSPHATE POTASSIUM PHOSPHATE, MONOBASIC 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 Foam Hand Sanitizer Alcohol Free 1000 mL (33.8 FL OZ) 4333B-V2PRDRevA17 image description
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.PACIFIC BLUE ULTRA Foam Hand Sanitizer Alcohol Free Fragrance Free SKU 43338 Manufactured for Georgia-Pacific Consumer Products LP. Atlanta, GA 30303 Questions? Call 1-866 HELLOGP (435-5647 or visit us on line at www.gppro.com 2017 Georgia-pacific Consumer Products LP. All rights reserved 43338-V1PRDRevA 146.000/146AA
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.Discontinue 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 do not use in or near eyes.
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