Active Ingredient:
Benzethonium Chloride 0.20%
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.
Benzethonium Chloride 0.20%
Antiseptic Handwash
Ask a doctor before use if you have , deep of puncture wounds, animal bites, serious burns
Store at room temperature (59°-86°F)
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
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