FDA.reportPublic FDA data

Summit 377Alcohol Free Foam Hand Sanitizer - R.L. Williams Company

Manufacturer
R.L. Williams Company
Effective date
2026-04-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:55:37

Label at a glance#

ProductSummit 377Alcohol Free Foam Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Pump a small amount of foam into palm of the hand. Rub thoroughly over all surfaces of both hands. Rub hands briskly until 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 decrease 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 the hand.
  • Rub thoroughly over all surfaces of both hands.
  • Rub hands briskly until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Phenoxyethanol, Lauramine Oxide, Panthenol, 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
1038799benzalkonium chloride 0.1 % Topical FoamPSN1
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD1
1038799benzalkonium chloride 0.1 % Topical FoamSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130810080570115GTIN-13: 0810080570115
EAN-13: 0810080570115
GTIN-12: 810080570115
UPC-A: 810080570115
GTIN storage (14 digits): 00810080570115		Summit377_Back.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23590-600-10Summit 377Alcohol Free Foam Hand Sanitizer850 mL in 1 BOTTLE, PUMPSOLUTION8501

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
23590-60023590-600-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
PANTHENOLWV9CM0O67ZIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
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 377Alcohol Free Foam Hand SanitizerBENZALKONIUM CHLORIDER.L. Williams Company50ae9765-2c2b-137f-e063-6294a90ae13a2026-04-30WarningsExact identifier
ndc (package): 23590-600-10
ndc (product): 23590-600
ndc11 (package): 23590060010
spl id: 50ae9765-2c2a-137f-e063-6294a90ae13a
spl set id: 50ae9765-2c2b-137f-e063-6294a90ae13a

Reported adverse events (FAERS/openFDA)#

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