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| Product NDC Code | 53125-817 | ||||
|---|---|---|---|---|---|
| Drug Name | North woods derma foam e-2 |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | SOAP | ||||
| RxCUI drug identifier | 1046593 | ||||
| Application Number | part333A | ||||
| Labeler Name | Superior Chemical Corporation | ||||
| 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 0.13%
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 Read the entire label before using this product. Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands for 15 seconds. Rinse with clean water.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients Water, coco-glucoside, laurtrimonium chloride, cocamidopropylamine oxide, citric acid.
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 the bacteria on the skin. Recommended for repeated use.
Purpose
Information about the drug product’s indications for use.Superior Derma Foam E2 Purpose Antimicrobial
Spl product data elements
Usually a list of ingredients in a drug product.North Woods Derma Foam E-2 Benzalkonium Chloride WATER LAURTRIMONIUM CHLORIDE BENZALKONIUM CHLORIDE BENZALKONIUM CAPRYLYL/CAPRYL OLIGOGLUCOSIDE ANHYDROUS CITRIC ACID
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.Superior Derma Foam E2 71729-00 Superior Derma Foam E2 71729-00 Superior Derma Foam
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.Superior Derma Foam E2 KEEP OUT OF REACH OF CHILDREN
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 eyes with water. Stop use and ask a doctor If irritation persists or redness deelops, or if 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