North Woods Derma Foam E-2 Soap
FDA Label NDC 53125-817

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 E-2 (NDC 53125-817). 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, superior derma foam e2, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

​Active Ingredient

Benzalkonium Chloride 0.13%

Indications & Usage

Uses

  • For handwashing to decrease the bacteria on the skin.
  • Recommended for repeated use.

Warnings

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.

Dosage & Administration

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

Inactive Ingredients

​Water, coco-glucoside, laurtrimonium chloride, cocamidopropylamine oxide, citric acid.

Superior Derma Foam E2

Purpose

Antimicrobial

KEEP OUT OF REACH OF CHILDREN

71729-00 Superior Derma Foam E2

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