Home NDC 68062-2243-2 Dr Lift Antibacterial
Product NDC 68062-2243
Requested package NDC 68062-2243-2
11-digit product format 680622243
Labeler code 68062
Product ID 68062-2243_40d7c6af-e655-d3e5-e063-6394a90af01c
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form LOTION
Route TOPICAL
Labeler Spa de Soleil
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-09-17
Substance BENZALKONIUM CHLORIDE
Active strength .156 mg/120mg
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 Dr Lift Antibacterial
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .156 mg/120mg
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 1046442 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68062-2243-1 Dr Lift Antibacterial 120 mg in 1 BOTTLE LOTION 120 2 68062-2243-2 Dr Lift Antibacterial 100 mg in 1 BOTTLE LOTION 100 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68062-2243 DR LIFT ANTIBACTERIAL (BENZALKONIUM CHLORIDE) LOTION [SPA DE SOLEIL] 1 Current NDC, Legacy NDC, 2 package rows 20200918_af89675e-e66f-0922-e053-2995a90ab9d2.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 9 of 115 · 2,286 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 68062-2243-2 68062224302 100 mg in 1 BOTTLE (68062-2243-2) 100 mg 2025-10-10 No No Current