FDA.reportPublic FDA data

Summit 367 Antibacterial Foam - R.L. Williams Company

Manufacturer
R.L. Williams Company
Effective date
2026-04-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:55:37

Label at a glance#

ProductSummit 367 Antibacterial Foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Pump a small amount of foam into palm of hand. Scrub thoroughly for at least 15 seconds. Rinse completely and dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For hand washing to help reduce bacteria on the skin

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.
  • Scrub thoroughly for at least 15 seconds.
  • Rinse completely and dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Phenoxyethanol, Fragrance, Citric Acid, Red 40, Blue 1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapPSN1
1233282benzalkonium chloride 1 MG/ML Medicated Liquid SoapSCD1
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130810080570009GTIN-13: 0810080570009
EAN-13: 0810080570009
GTIN-12: 810080570009
UPC-A: 810080570009
GTIN storage (14 digits): 00810080570009		Summit367_Back.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23590-200-10Summit 367 Antibacterial Foam850 mL in 1 BOTTLE, PUMPSOLUTION8501

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
23590-20023590-200-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
FD&C RED NO. 40WZB9127XOAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
PHENOXYETHANOLHIE492ZZ3TIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

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 367 Antibacterial FoamBENZALKONIUM CHLORIDER.L. Williams Company509f2491-ea17-86ee-e063-6394a90a59402026-04-29WarningsExact identifier
ndc (package): 23590-200-10
ndc (product): 23590-200
ndc11 (package): 23590020010
spl id: 509f01c4-79a0-69d4-e063-6394a90a4a83
spl set id: 509f2491-ea17-86ee-e063-6394a90a5940

Reported adverse events (FAERS/openFDA)#

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