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North woods derma foam e-2 - Medication Information

Product NDC Code 53125-817
Drug Name

North woods derma foam e-2

Type Brand
Active Ingredients
Benzalkonium chloride 1.3 mg/ml
Route TOPICAL
Dosage Form SOAP
Application Number 505G(a)(3)
Labeler Name Superior Chemical Corporation
Packages
Package NDC Code Description
53125-817-29 1000 ml in 1 bag (53125-817-29)
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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 GLYCERIN SODIUM BENZOATE ALCOHOL TETRASODIUM EDTA 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