SSDC Foaming Hand Sanitizer

Manufacturer: Ecolab Inc.
Effective date: 2026-03-04
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:48:56

Label at a glance#

ProductSSDC Foaming Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Indications and uses

For handwashing to decrease bacteria on the skin

Dosage and administration

Wash hands to remove soil Dispense palmful Spread to cover hands, rub in well Air dry, do not rinse or towel dry

Contacts and useful links#

PhoneLabel contact(877) 231-2615

PhoneLabel contact(952) 853-1713

PhoneLabel contact1-800-532-7732

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

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 this product

OTC - WHEN USING SECTION

If in eyes, rinse promptly and thoroughly with water
Discontinue use if irritation and redness develop

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

Skin irritation and 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

Wash hands to remove soil
Dispense palmful
Spread to cover hands, rub in well
Air dry, do not rinse or towel dry

Other Information

REFERENCES SECTION

for additional information, see Material Safety Data Sheet (MSDS)
For emergency medical information in USA, call (877) 231-2615 or call collect 0 (952) 853-1713

INACTIVE INGREDIENT SECTION

Inactive ingredients water (aqua), isopropyl alcohol, propylene glycol, CI 16035 (FD&C Red 40), CI 42090 (FD&C Blue 1)

OTC - QUESTIONS SECTION

Questions? Call 1-800-532-7732

Principal display panel and representative container

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SSDC FOAMING HAND SANITIZER
KEEP OUT OF REACH OF CHILDREN

Benzalkonium chloride 0.1%
Net Contents:
1200 mL (47.24 US FL OZ)
785082/7300/1025

representative label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1038799	benzalkonium chloride 0.1 % Topical Foam	PSN	1
1038799	benzalkonium chloride 1 MG/ML Topical Foam	SCD	1
1038799	benzalkonium chloride 0.1 % Topical Foam	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
47593-662-70	SSDC Foaming Hand Sanitizer	1250 mL in 1 BOTTLE, PLASTIC	SOLUTION	1250		1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

SSDC Foaming Hand Sanitizer
Benzalkonium Chloride
BENZALKONIUM
WATER
ISOPROPYL ALCOHOL
PROPYLENE GLYCOL
FD&C RED NO. 40
FD&C BLUE NO. 1

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
47593-662	47593-662-70

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SSDC Foaming Hand Sanitizer	BENZALKONIUM CHLORIDE	Ecolab Inc.	c4063012-34ab-4409-baf4-9e3d8f3e2011	2026-03-04	Warnings	Exact identifier ndc (package): 47593-662-70 ndc (product): 47593-662 ndc11 (package): 47593066270 spl id: 97346bba-3ef3-4124-945b-e3e331e474b7 spl set id: c4063012-34ab-4409-baf4-9e3d8f3e2011

Reported adverse events (FAERS/openFDA)#

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