Summit 377Alcohol Free Foam Hand Sanitizer

Product NDC
23590-600
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 Identifiers#

Field, Values table
FieldValues
UniiF5UM2KM3W7
Rxcui1038799

DailyMed Package Descriptions#

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

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