Home NDC 68062-2242 Dr Lift Antibacterial Hand Wash
Product NDC 68062-2242
11-digit product format 680622242
Labeler code 68062
Product ID 68062-2242_50b719c9-4516-85fd-e063-6294a90a9103
Type HUMAN OTC DRUG
Nonproprietary name benzalkonium chloride
Dosage form GEL
Route TOPICAL
Labeler Spa de Soleil
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-07-29
Substance BENZALKONIUM CHLORIDE
Active strength .46 mg/240mg
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 18 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 68062-2242-1 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 68062-2242-1 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 68062-2242-1 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 68062-2242-1 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 68062-2242-1 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 68062-2242-1 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 68062-2242-1 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 68062-2242-1 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 68062-2242-1 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 Hand Wash
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .46 mg/240mg
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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68062-2242-1 Dr Lift Antibacterial Hand Wash 240 mg in 1 TUBE GEL 240 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68062-2242 DR LIFT ANTIBACTERIAL HAND WASH (BENZALKONIUM CHLORIDE) GEL [SPA DE SOLEIL] 1 Current NDC, Legacy NDC, 1 package rows 20200730_ab9e2c3c-d422-255e-e053-2a95a90a7a22.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 96 of 114 · 2,277 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join DK12 Shower Gel Fresh Energy BENZALKONIUM CHLORIDE 0.13% Industria La Popular, S.A. 05e4ff0e-ef63-ef3b-e063-6294a90aa2b8 2024-12-02 Warnings Exact identifier application number: M003 DK12 Vitamin E Antibacterial and Moisturizing BENZALKONIUM CHLORIDE 0.1% Industria La Popular, S.A. fe9270c0-bf6b-f0ff-e053-6394a90ae8f1 2024-12-02 Warnings Exact identifier application number: M003 DK12 Liquid Hand Creamy BENZALKONIUM CHLORIDE 0.13% Industria La Popular, S.A. 01e2e51b-212b-368e-e063-6294a90a871c 2024-12-02 Warnings Exact identifier application number: M003 DK12 Fresh Energy Antibacterial and Moisturizing BENZALKONIUM CHLORIDE 0.1% Industria La Popular, S.A. fe80635d-9594-abf3-e053-6394a90aa78b 2024-12-02 Warnings Exact identifier application number: M003 DK12 Shower Gel Creamy BENZALKONIUM CHLORIDE 0.13% Industria La Popular, S.A. 05e36111-ed4e-12de-e063-6294a90af639 2024-12-02 Warnings Exact identifier application number: M003 DK12 Creamy Antibacterial and Moisturizing BENZALKONIUM CHLORIDE 0.1% Industria La Popular, S.A. fe7fde7e-82fc-c13f-e053-6394a90aff68 2024-12-02 Warnings Exact identifier application number: M003 DK12 Oatmeal Antibacterial and Moisturizing BENZALKONIUM CHLORIDE 0.1% Industria La Popular, S.A. fe16387b-1b16-1f41-e053-6294a90ae2c0 2024-12-02 Warnings Exact identifier application number: M003 First Aid Antiseptic Isopropyl Alcohol Pad ISOPROPYL ALCOHOL Fourstar Group USA, Inc. 27edf5dc-3e68-bdd0-e063-6394a90ac485 2024-11-27 Warnings Exact identifier application number: M003 MicroKlenz Antimicrobial BENZETHONIUM CHLORIDE Medline Industries, LP 115dda08-709c-490a-9693-419b51441960 2024-11-26 Warnings Exact identifier application number: M003 First Aid Only Alcohol Antiseptic Pad ALCOHOL PAD Acme United Corporation 55421010-d806-4ca4-e054-00144ff88e88 2024-11-26 Warnings Exact identifier application number: M003 First Aid Only Hydrogen Peroxide 3% HYDROGEN PEROXIDE Acme United Corporationn f1db8929-9b95-0d6e-e053-2995a90a817f 2024-11-26 Warnings Exact identifier application number: M003 First Aid Only Sting Relief Pad BENZOCAINE, ISOPROPYL ALCOHOL Acme United Corporation d71047f6-1353-c758-e053-2995a90a962c 2024-11-26 Warnings Exact identifier application number: M003 First Aid Only Alcohol Antiseptic Pad ISOPROPYL ALCOHOL Acme United Coporation a01fec1b-1339-40b9-e053-2995a90aeda5 2024-11-23 Warnings Exact identifier application number: M003 Med-Nap Sterile Alcohol Prep Pads ISOPROPYL ALCOHOL Acme United Corporation c6eff57b-d537-69c8-e053-2a95a90adc3a 2024-11-23 Warnings Exact identifier application number: M003 First Aid Only Alcohol Antiseptic ISOPROPYL ALCOHOL Acme United Corporation a810e723-ad0c-8c71-e053-2995a90a0acc 2024-11-23 Warnings Exact identifier application number: M003 Universal 50% Rubbing Alcohol ISOPROPYL ALCOHOL Universal Distribution Center LLC 0dcc9bd2-aea5-4c27-9956-47d56221726b 2024-11-22 Warnings Exact identifier application number: M003 Universal 70% Rubbing Alcohol with Wintergreen and Glycerin ISOPROPYL ALCOHOL Universal Distribution Center LLC 9a9d42ad-79d5-4acc-b5d9-cb7468961d47 2024-11-22 Warnings Exact identifier application number: M003 Universal 50% Rubbing Alcohol with Wintergreen and Glycerin ISOPROPYL ALCOHOL Universal Distribution Center LLC 044a6287-f568-4cfa-a813-7fc0e6ffc352 2024-11-22 Warnings Exact identifier application number: M003 NEXXGEN 70% RUBBING ALCOHOL ISOPROPYL ALCOHOL A & A Nexxgen LLC ce73ac48-c5af-4a35-950c-62ff0232aa30 2024-11-22 Warnings Exact identifier application number: M003 Universal 70% Rubbing Alcohol ISOPROPYL ALCOHOL Universal Distribution Center LLC d8b9b0e7-2cb8-4fc5-af55-790e64d6cfe8 2024-11-22 Warnings Exact identifier application number: M003
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68062-2242-1 68062224201 240 mg in 1 TUBE (68062-2242-1) 240 mg 2020-07-29 0000-00-00 No No Current