Summit 377Alcohol Free Foam Hand Sanitizer

Product NDC
23590-600
Requested package NDC
23590-600-10
11-digit product format
235900600
Labeler code
23590
Product ID
23590-600_50ae9765-2c2a-137f-e063-6294a90ae13a
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
SOLUTION
Route
TOPICAL
Labeler
R.L. Williams Company
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-04-30
Substance
BENZALKONIUM CHLORIDE
Active strength
1 mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Summit 377Alcohol Free Foam Hand Sanitizer
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE1 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F5UM2KM3W7Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1038799Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
50ae9765-2c2b-137f-e063-6294a90ae13aAvailable on FDA.report

DailyMed Package Descriptions#

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

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN50ae9765-2c2b-137f-e063-6294a90ae13a1
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD50ae9765-2c2b-137f-e063-6294a90ae13a1
1038799benzalkonium chloride 0.1 % Topical FoamSY50ae9765-2c2b-137f-e063-6294a90ae13a1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
23590-600-1023590060010850 mL in 1 BOTTLE, PUMP (23590-600-10) 850 ml2026-04-30NoNoCurrent