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 94 of 114 · 2,277 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join NEXXGEN 70% RUBBING ALCOHOL with Wintergreen ISOPROPYL ALCOHOL A & A Nexxgen LLC 8d1a5c98-8169-4f40-8601-a6f6bbbbebe7 2024-12-09 Warnings Exact identifier application number: M003 NEXXGEN 91% RUBBING ALCOHOL with Wintergreen ISOPROPYL ALCOHOL A & A Nexxgen LLC 12b8c85a-da0c-47a1-9531-c9f2858c4f31 2024-12-09 Warnings Exact identifier application number: M003 NEXXGEN 91% RUBBING ALCOHOL ISOPROPYL ALCOHOL A & A Nexxgen LLC 609267da-3ee6-4bd3-aecf-610d9047774c 2024-12-09 Warnings Exact identifier application number: M003 Isopropyl Alcohol ISOPROPYL ALCOHOL Sarnova, Inc. 62be13a6-da24-4ab0-b0f4-f2894324c20c 2024-12-06 Warnings Exact identifier application number: M003 Instant Hand Antiseptic ALCOHOL ASP Global b84075db-be0c-4265-b262-825bc6ade9d8 2024-12-06 Warnings Exact identifier application number: M003 Instant Hand Antiseptic BENZALKONIUM CHLORIDE ASP Global 47276148-08e5-400e-94ac-d2d9db423b51 2024-12-06 Warnings Exact identifier application number: M003 Instant Hand Antiseptic ALCOHOL ASP Global 9aca3f89-cdde-430c-8eb6-43a3ac3fc0df 2024-12-06 Warnings Exact identifier application number: M003 Instant Hand Antiseptic BENZALKONIUM CHLORIDE ASP Global 4eef4b0f-9209-45a4-8a0e-7891fc380fe5 2024-12-05 Warnings Exact identifier application number: M003 MERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 1.5 BENZETHONIUM CHLORIDE Yangzhou H&R Plastic Daily Chemical Co., Ltd. 2998b2bd-6208-4cb4-982b-0ffb97d7d75d 2024-12-05 Warnings Exact identifier application number: M003 MERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 0.5 BENZETHONIUM CHLORIDE Yangzhou H&R Plastic Daily Chemical Co., Ltd. 68003c71-5959-476f-b252-1f131e9305e2 2024-12-05 Warnings Exact identifier application number: M003 MERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 3 BENZETHONIUM CHLORIDE Yangzhou H&R Plastic Daily Chemical Co., Ltd. e35e468a-1f0c-4a3f-ac6a-cd55a72f3cc2 2024-12-05 Warnings Exact identifier application number: M003 MERIDIAN UNWARPPED ANTIBACTERIAL DEODORANT 3 OZ BENZETHONIUM CHLORIDE Yangzhou H&R Plastic Daily Chemical Co., Ltd. b621b4cd-20db-44d8-b114-a977deea8eb4 2024-12-05 Warnings Exact identifier application number: M003 MERIDIAN WARPPED ANTIBACTERIAL DEODORANT 0.5 BENZETHONIUM CHLORIDE Yangzhou H&R Plastic Daily Chemical Co., Ltd. c3a053ba-65fe-4540-9c81-29700cda5efa 2024-12-05 Warnings Exact identifier application number: M003 MERIDIAN WARPPED ANTIBACTERIAL DEODORANT 3 OZ BENZETHONIUM CHLORIDE Yangzhou H&R Plastic Daily Chemical Co., Ltd. 2989afeb-8451-4a72-8456-195cd5117a41 2024-12-05 Warnings Exact identifier application number: M003 MERIDIAN WARPPED ANTIBACTERIAL DEODORANT 1.25 BENZETHONIUM CHLORIDE Yangzhou H&R Plastic Daily Chemical Co., Ltd. 17092ebf-8e57-4e1a-9bba-87a662c361c0 2024-12-05 Warnings Exact identifier application number: M003 MERIDIAN WARPPED ANTIBACTERIAL DEODORANT 3 BENZETHONIUM CHLORIDE Yangzhou H&R Plastic Daily Chemical Co., Ltd. 3ed3332e-f888-4b9c-aab7-99f8719b835e 2024-12-05 Warnings Exact identifier application number: M003 OPS 70 PERCENT ALCOHOL FOAMING SKIN SANITIZER ETHYL ALCOHOL Archer Manufacturing, Inc. d05fbe85-26de-0d24-e053-2a95a90ab5cb 2024-12-05 Warnings Exact identifier application number: M003 OPS AB ANTIBACTERIAL FOAMING BENZALKONIUM CHLORIDE Archer Manufacturing, Inc. 615921dd-46e5-403c-9ed3-f30beb0c0bb9 2024-12-05 Warnings Exact identifier application number: M003 BLACK OPS 70 PERCENT ALCOHOL FOAMING SKIN SANITIZER ETHYL ALCOHOL Archer Manufacturing, Inc. d334b7f0-01dc-7f59-e053-2a95a90a06b5 2024-12-05 Warnings Exact identifier application number: M003 BLACK OPS INSTANT HAND SANITIZER BENZALKONIUM CHLORIDE Archer Manufacturing, Inc. d3366750-18b8-1194-e053-2995a90a4359 2024-12-05 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