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North woods derma foam hand sanitizer - Medication Information

Product NDC Code 53125-700
Drug Name

North woods derma foam hand sanitizer

Type Brand
Active Ingredients
Benzalkonium chloride 1.3 mg/ml
Route TOPICAL
Dosage Form SOAP
RxCUI drug identifier 1020365
Application Number part333A
Labeler Name Superior Chemical Corporation
Packages
Package NDC Code Description
53125-700-54 1000 ml in 1 bag (53125-700-54)
53125-700-57 550 ml in 1 bottle, pump (53125-700-57)
53125-700-88 500 ml in 1 bottle, pump (53125-700-88)
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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 product onto dry hands. Rub hands together until hands are dry. Use as needed between hand washes to reduce bacteria on the skin.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Deionized ​Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone, DMDM Hydantoin, PEG-3 Cocamide, Fragrance, Iodoproynyl Btylcarbamate, D&C Green #5.

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 Use in a variety of public facilities. Use this product when soap and water are not available.

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.
North Woods Derma Foam Hand Sanitizer Benzalkonium Chloride WATER SODIUM PYRROLIDONE CARBOXYLATE POLYETHYLENE GLYCOL 400 DIMETHICONE DMDM HYDANTOIN PEG-3 COCAMINE IODOPROPYNYL BUTYLCARBAMATE D&C GREEN NO. 5 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.
Superior Derma Foam Hand Sanitizer 75229-00_Superior Derma Foam Hand Sanitizer. 75229 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.
KEEP OUT OF REACH OF CHILDREN

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or Comments? Phone: (800) 777-9343 MDS information: ​(800) 891-4965

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. Avoid contact with eyes. Children under the age of 6 should be supervised by an adult when using this product. Discontinue use is irritation or redness develops. If irritation persists for more than 72 hours, consult a physician. KEEP OUT OF REACH OF CHILDREN .

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