FDA.reportPublic FDA data

Summit E2

Manufacturer
R.L. Williams Company
Effective date
2026-03-19
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:51:03

Label at a glance#

ProductSummit E2
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

Reduces amount of bacteria on hands Recommended for repeated use

Dosage and administration

Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands for at least 15 seconds. Rinse with potable water.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Skin Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Reduces amount of bacteria on hands
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

When using this product, avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists 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

  • Pump a small amount of foam into palm of hand.
  • Rub thoroughly over all surfaces of both hands for at least 15 seconds.
  • Rinse with potable water.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Phenoxyethanol, Citric Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label - 850 mL Cartridge (Front)Package Label - 850 mL Cartridge (Front)

Package Label - 850 mL Cartridge (Back)Package Label - 850 mL Cartridge (Back)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapPSN5
1233282benzalkonium chloride 1 MG/ML Medicated Liquid SoapSCD5
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapSY5

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130810080570047GTIN-13: 0810080570047
EAN-13: 0810080570047
GTIN-12: 810080570047
UPC-A: 810080570047
GTIN storage (14 digits): 00810080570047		summite2back_850.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23590-300-10Summit E2850 mL in 1 BOTTLE, PUMPSOAP8505

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
23590-30023590-300-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
LAURAMINE OXIDE4F6FC4MI8WIACT
WATER059QF0KO0RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
Summit E2BENZALKONIUM CHLORIDER.L. Williams Companydec25905-5b08-4866-a2a5-4c60409761fc2026-03-19WarningsExact identifier
ndc (package): 23590-300-10
ndc (product): 23590-300
ndc11 (package): 23590030010
spl id: 4d66824a-b004-e0c5-e063-6394a90a82f5
spl set id: dec25905-5b08-4866-a2a5-4c60409761fc

Reported adverse events (FAERS/openFDA)#

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