Home NDC 21749-454-90 Primory Antibacterial Plum Foam Handwash
Product NDC 21749-454
Requested package NDC 21749-454-90
11-digit product format 217490454
Labeler code 21749
Product ID 21749-454_2929f990-d526-ca02-e063-6394a90adf4d
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form LIQUID
Route TOPICAL
Labeler GOJO Industries, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-06-14
Substance BENZALKONIUM CHLORIDE
Active strength .5 mg/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Primory Antibacterial Plum Foam Handwash
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .5 mg/100mL
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 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 21749-454-08 Primory Antibacterial Plum Foam Handwash 236 mL in 1 PACKAGE LIQUID 236 4 21749-454-89 Primory Antibacterial Plum Foam Handwash 1200 mL in 1 PACKAGE LIQUID 1200 4 21749-454-90 Primory Antibacterial Plum Foam Handwash 1250 mL in 1 PACKAGE LIQUID 1250 4 21749-454-97 Primory Antibacterial Plum Foam Handwash 700 mL in 1 PACKAGE LIQUID 700 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21749-454 PRIMORY ANTIBACTERIAL PLUM FOAM HANDWASH (BENZALKONIUM CHLORIDE) LIQUID [GOJO INDUSTRIES, INC.] 4 Current NDC, Legacy NDC, 4 package rows 20241215_3459ed2b-9440-4139-9262-f055d3980af7.zip
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 21749-454-90 21749045490 1250 mL in 1 PACKAGE (21749-454-90) 1250 ml 2017-06-14 0000-00-00 No No Current