Home NDC 83986-224 Foaming Hand
Product NDC 83986-224
11-digit product format 839860224
Labeler code 83986
Product ID 83986-224_4cc4089a-07cb-f08f-e063-6394a90a1625
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form SOAP
Route TOPICAL
Labeler UpLift Brands, LLC
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-04-11
Substance BENZALKONIUM CHLORIDE
Active strength 1.3 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 Foaming Hand
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 1.3 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 1046593 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 83986-224-08 Foaming Hand 3785 mL in 1 BOTTLE, PLASTIC SOAP 3785 4 83986-224-45 Foaming Hand 1150 mL in 1 BOTTLE, PLASTIC SOAP 1150 4 83986-224-86 Foaming Hand 1000 mL in 1 BOTTLE, DISPENSING SOAP 1000 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83986-224 FOAMING HAND (BENZALKONIUM CHLORIDE) SOAP [UPLIFT BRANDS, LLC] 3 Current NDC, 3 package rows 20250416_a4bdb4a3-5706-4676-a6d3-22971f023dba.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83986-224-08 83986022408 3785 mL in 1 BOTTLE, PLASTIC (83986-224-08) 3785 ml 2024-04-11 No No Current 83986-224-45 83986022445 1150 mL in 1 BOTTLE, PLASTIC (83986-224-45) 1150 ml 2024-04-11 No No Current 83986-224-86 83986022486 1000 mL in 1 BOTTLE, DISPENSING (83986-224-86) 1000 ml 2024-04-11 No No Current