Home NDC 23590-200-10 Summit 367 Antibacterial Foam
Product NDC 23590-200
Requested package NDC 23590-200-10
11-digit product format 235900200
Labeler code 23590
Product ID 23590-200_509f01c4-79a0-69d4-e063-6394a90a4a83
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 2026-04-29
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 367 Antibacterial Foam
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 1 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F5UM2KM3W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1233282 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 23590-200-10 Summit 367 Antibacterial Foam 850 mL in 1 BOTTLE, PUMP SOLUTION 850 1
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 23590-200-10 23590020010 850 mL in 1 BOTTLE, PUMP (23590-200-10) 850 ml 2026-04-29 No No Current