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 98 of 114 · 2,277 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join MED NAP Cleansing Towelette BENZALKONIUM CHLORIDE Acme United Corporation d92cd45a-234c-4872-e053-2a95a90a3e1c 2024-11-09 Warnings Exact identifier application number: M003 MED NAP Obstetrical Towelette BENZALKONIUM CHLORIDE Acme United Corporation d83d2fab-6972-9b18-e053-2995a90a5cb5 2024-11-09 Warnings Exact identifier application number: M003 MED NAP Benzalkonium Chloride Antiseptic BENZALKONIUM CHLORIDE Acme United Corporation d7c404c1-c765-a67c-e053-2995a90a6b8e 2024-11-09 Warnings Exact identifier application number: M003 Barbie BZK ANTISEPTIC WIPE BENZALKONIUM CHLORIDE Ashtel Studios, Inc. d675eb91-80a8-4874-a2b0-c2bf69264911 2024-11-08 Warnings Exact identifier application number: M003 Barbie ALCOHOL WIPE ISOPROPYL ALCOHOL Ashtel Studios, Inc. a4a6beb0-5781-4d74-9120-7ca64e035c23 2024-11-08 Warnings Exact identifier application number: M003 MARVEL ALCOHOL WIPE ISOPROPYL ALCOHOL Ashtel Studios, Inc. f6cd4757-d6e0-46bd-827f-3f380c71858f 2024-11-07 Warnings Exact identifier application number: M003 Instant Hand Sanitizer HAND SANITIZER Raining Rose, Inc. 2656d129-df88-4489-e063-6394a90a4b49 2024-11-07 Warnings Exact identifier application number: M003 HealthWise Advanced Hand Sanitizer ETHYL ALCOHOL 70% Veridian Healthcare 261bd056-c2f9-2a69-e063-6394a90af8df 2024-11-04 Warnings Exact identifier application number: M003 Hand Sanitizer Cucumber Aloe ORGANIC ETHYL ALCOHOL Whole Foods Market, Inc. 0588ae1b-f29a-e1b6-e063-6394a90a0de1 2024-11-02 Warnings Exact identifier application number: M003 Hand Sanitizer Cucumber Aloe ETHYL ALCOHOL Whole Foods Market, Inc. 074334af-c26e-4126-e063-6394a90ae4c4 2024-11-02 Warnings Exact identifier application number: M003 Hand Sanitizer Orange Blossom ORGANIC ETHYL ALCOHOL Whole Foods Market, Inc. 07f708d1-11c8-eb50-e063-6294a90a3a81 2024-11-02 Warnings Exact identifier application number: M003 Hand Sanitizer Lavender ETHYL ALCOHOL Whole Foods Market, Inc. 0742f251-5fc9-c015-e063-6394a90a79b1 2024-11-02 Warnings Exact identifier application number: M003 Hand Sanitizer Orange Blossom ETHYL ALCOHOL Whole Foods Market, Inc. 07436407-7a15-7cee-e063-6294a90a9651 2024-11-02 Warnings Exact identifier application number: M003 Hand Sanitizer Lavender ETHYL ALCOHOL Whole Foods Market, Inc. 07f7e966-e57e-dede-e063-6294a90acbf5 2024-11-02 Warnings Exact identifier application number: M003 Hand Sanitizer Lavender ETHYL ALCOHOL Whole Foods Market, Inc. ec8c7597-a3f1-65a8-e053-2995a90a69a1 2024-11-02 Warnings Exact identifier application number: M003 Lemongrass Hand Sanitizer ALCOHOL Natural Essentials, Inc. 25ca3908-24aa-5e4f-e063-6394a90a7a88 2024-10-31 Warnings Exact identifier application number: M003 Sanar Naturals Decolorized Iodine ETHYL ALCOHOL Sanvall Enterprises, Inc 16c92427-84d2-cad5-e063-6394a90af435 2024-10-31 Warnings Exact identifier application number: M003 Sanar Naturals Mercurochrome BENZALKONIUM CHLOLRIDE Sanvall Enterprises, Inc 16c6c2f0-0f08-e640-e063-6394a90aa01d 2024-10-31 Warnings Exact identifier application number: M003 Sanar Naturals Gentian Violet GENTIAN VIOLET Sanvall Enterprises, Inc 1922518d-e49b-5010-e063-6394a90a9112 2024-10-31 Warnings Exact identifier application number: M003 Lavender Hand Sanitizer ALCOHOL Natural Essentials, Inc. 25cada8c-8c80-c140-e063-6294a90a3336 2024-10-31 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