North Woods Derma Foam Hand Sanitizer Soap
FDA Label NDC 53125-700

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Superior Chemical Corporation for the product North Woods Derma Foam Hand Sanitizer (NDC 53125-700). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, indications & usage, warnings, dosage & administration, inactive ingredient, otc - questions, otc - purpose, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

​Active Ingredient

Benzalkonium Chloride 0.13%

Indications & Usage

Uses

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

Warnings

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.

Dosage & Administration

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

Inactive Ingredients

Deionized ​Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone, DMDM Hydantoin, PEG-3 Cocamide, Fragrance, Iodoproynyl Btylcarbamate, D&C Green #5.

Otc - Questions

Questions or Comments?Phone: (800) 777-9343

MDS information:​(800) 891-4965

Otc - Purpose

Purpose

Antiseptic

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

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