SSDC ANTIBACTERIAL FOAM HANDSOAP

Manufacturer
Ecolab Inc. | Ecolab LLC
Effective date
2026-03-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:48:54

Label at a glance#

ProductSSDC ANTIBACTERIAL FOAM HANDSOAP
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

for handwashing to decrease bacteria on the skin

Dosage and administration

wet hands and apply foam scrub hands and forearms rinse thoroughly and dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.5%

Purpose

OTC - PURPOSE SECTION

Antiseptic handwash

Uses

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • in eyes

When using the product

OTC - WHEN USING SECTION

  • if in eyes, rinse promptly and thoroughly with water 
  • discontinue use if irritation and redness develop

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if skin irritation or redness occurs for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands and apply foam
  • scrub hands and forearms
  • rinse thoroughly and dry

Other information

REFERENCES SECTION

  • 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 SECTION

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

OTC - QUESTIONS SECTION

Questions? call 1-800-532-7732

Principal display panel & representative package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SSDC ANTIBACTERIAL FOAM HANDSOAP

1113028

1200 mL (47.24 US FL OZ)

Active ingredient:

Benzalkonium chloride 0.5%

785099/7300/1025

Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA

© 2025 Kay Chemical Company · All rights reserved

Made in U.S.A.

representative labelrepresentative label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1731737benzalkonium chloride 0.5 % Medicated Liquid SoapPSN1
1731737benzalkonium chloride 5 MG/ML Medicated Liquid SoapSCD1
1731737benzalkonium chloride 0.5 % Medicated Liquid SoapSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47593-663-70SSDC ANTIBACTERIAL FOAM HANDSOAP1200 mL in 1 BOTTLE, PLASTICSOLUTION12001

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47593-66347593-663-70

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SSDC ANTIBACTERIAL FOAM HANDSOAPBENZALKONIUM CHLORIDEEcolab Inc.a2a4e9d1-d63a-476b-a048-d360104e36882026-03-03WarningsExact identifier
ndc (package): 47593-663-70
ndc (product): 47593-663
ndc11 (package): 47593066370
spl id: f69d870e-1eba-4623-ac25-e8fbb0a66e8f
spl set id: a2a4e9d1-d63a-476b-a048-d360104e3688

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.