Hand-e-foam
FDA Label NDC 61924-102

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dermarite Industries, Llc for the product Hand-e-foam (NDC 61924-102). 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 active ingredient:, purpose:, uses:, warnings:, warnings, directions:, other information:, inactive ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient:

Benzethonium Chloride 0.20%

Purpose:

Antiseptic Handwash

Uses:

  • Hand sanitizer: Helps reduce bacteria on skin that could cause disease. Recommended for repeated use.
  • First aid to help protect against skin infection in minor cuts, scrapes, burns.

Warnings:

  • For external use only.
  • Avoid contact with eyes. In case of contact, flush thoroughly with water.
  • When using this product do not apply to large area of raw or blistered skin in large quantities; do not use in or near the eyes. 
  • Ask a doctor before use if you have , deep of puncture wounds, animal bites, serious burns

Warnings

  • Keep out of reach of children. In case of accidental ingestion contact a physician or Poison Control Center right away

Directions:

  • Hand sanitizer: Wet hands thoroughly with product and allow to dry without wiping. Children should be supervised when using this product.
  • First Aid: Clean the affected area whenever possible. Apply to affected area not more than 3 to 4 times daily. May be covered with a sterile bandage:if bandaged, let dry first.

Other Information:

Store at room temperature (59°-86°F)

Inactive Ingredients:

Benzalkonium Chloride, Cetrimonium Chloride, Diazolidinyl Urea, Fragrance, Glycerin, Hydroxethyl Cetyldimonium Phosphate, Methylchloroisothiazolinone, Methylisothiazolinone, Methylparaben, PEG-40 Dimethicone, PEG-40 Hydrogenated Castor Oil, PEG-8 Ricinoleate, Propylene Glycol, Propylparaben, Sodium Hydroxide, Tocopheryl Acetate, Water

Hand-E-Foam Package Label Principal Display Panel

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