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OTC products · Product label record

Swisher Advanced Antibacterial Foam Handsoap drug information

BENZALKONIUM CHLORIDE
Ecolab Inc. · TOPICAL

Product NDC: 47593-696

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameBENZALKONIUM CHLORIDE
Labeler / manufacturerEcolab Inc.
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC47593-696
Label effective date2026-08-31

Official product label reference

Swisher Advanced Antibacterial Foam Handsoap — Ecolab Inc.

This page contains 12 source sections for BENZALKONIUM CHLORIDE, topical route. Label set 38bd6680-db95-424c-8e84-2e12c2388a73, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses for handwashing to decrease bacteria on the skin

Purpose

Purpose Antiseptic handwash
Dosage and administration — label text
Directions wet hands and apply foam scrub hands and forearms rinse thoroughly and dry
Warnings
Warnings For external use only Do not use in eyes When using the product if in eyes, rinse promptly and thoroughly with water discontinue use if irritation and redness develop Stop use and ask a doctor if skin irritation or redness occurs for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Active ingredient
Active Ingredient Benzalkonium chloride 0.5%
Do not use
Do not use in eyes
While using this medicine
When using the product if in eyes, rinse promptly and thoroughly with water discontinue use if irritation and redness develop
Ask a doctor before use
Stop use and ask a doctor if skin irritation or redness occurs for more than 72 hours
Child safety
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
References
Other information READ SAFETY DATA SHEET (SDS) BEFORE USING THIS PRODUCT EMERGENCY HEALTH INFORMATIN: 1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US).
Inactive ingredient
Inactive ingredients water (aqua), cocamine oxide, hexylene glycol, PEG-180, glycerin, cocamidopropyl , PG-dimonium chloride phosphate, phenoxyethanol, polyquaternium-7, myristamide DIPA, myristamine oxide, citric acid, methyl gluceth-20, glyceryl caprylate/caprate, alcohol, PEG-12 dimethicone, potassium citrate, fragrance, blue 1
Questions
Questions? call 1.800.352.5326

Official sources and product identifiers

Substances listed: BENZALKONIUM CHLORIDE

RxNorm identifiers: 1731737

Package NDC codes

47593-696-41

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.