Home NDC 68062-2243 Dr Lift Antibacterial
Product NDC 68062-2243
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 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 · 16 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 2025-08-27 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 68062-2243-1 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 68062-2243-1 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 68062-2243-1 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 68062-2243-1 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 68062-2243-1 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 68062-2243-1 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 68062-2243-1 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 68062-2243-1 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
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 86 of 114 · 2,277 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join XtraCare Cucumber Melon ETHYL ALCOHOL Rejoice International 021fa2a0-d2ea-4699-a3d8-3c0af18c5aa3 2025-02-12 Warnings Exact identifier application number: M003 XtraCare Lavender Chamomile ETHYL ALCOHOL Rejoice International 6e611e87-1835-49f8-aa52-b724bd251527 2025-02-12 Warnings Exact identifier application number: M003 XtraCare Sweet Pea Blossom ETHYL ALCOHOL Rejoice International 1a5408f2-910c-4c6a-b6b3-c1304dd1cdf0 2025-02-12 Warnings Exact identifier application number: M003 XtraCare Warm Vanilla ETHYL ALCOHOL Rejoice International 46e7b4fa-3722-4487-9325-f8552ea92acf 2025-02-12 Warnings Exact identifier application number: M003 Instant Hand Sanitizer 2oz Bonus pack ETHYL ALCOHOL Rejoice International Inc. 5b209df6-d896-170c-e053-2a91aa0a52a8 2025-02-12 Warnings Exact identifier application number: M003 Hand Sanitizer w/ Carabiner (Strawberry Scented) 2oz Bonus pack ETHYL ALCOHOL Rejoice International Inc. 6e62eb50-ebb8-361e-e053-2991aa0aba6f 2025-02-12 Warnings Exact identifier application number: M003 Hand Sanitizer w/ Carabiner (Lemon Scented) 2oz Bonus pack ETHYL ALCOHOL Rejoice International Inc. 6e6585a3-61e1-30ec-e053-2a91aa0a6039 2025-02-12 Warnings Exact identifier application number: M003 Smart Care Assorted Licensed Sanitizer Spider Man 01 ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 2dedab76-3f5a-febf-e063-6394a90a6993 2025-02-12 Warnings Exact identifier application number: M003 Hand Sanitizer w/ Carabiner (Watermelon Scented) 2oz Bonus pack ETHYL ALCOHOL Rejoice International Inc. 6e65856c-0e14-1ab6-e053-2991aa0a3f3e 2025-02-12 Warnings Exact identifier application number: M003 Smart Care Assorted Licensed Sanitizer Barbie 01 ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 2dfd2ffd-a85a-f63e-e063-6294a90a6a5e 2025-02-12 Warnings Exact identifier application number: M003 Smart Care Assorted Licensed Sanitizer Crayola 01 ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 2dfd4acb-451b-12d3-e063-6294a90a4873 2025-02-12 Warnings Exact identifier application number: M003 Smart Care Assorted Licensed Sanitizer Hot Wheels 01 ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 2dfdd225-24f4-6d57-e063-6394a90a8a24 2025-02-12 Warnings Exact identifier application number: M003 Smart Care Cucumber Melon Hand Sanitizer 01 ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 2dfe0ac7-99d5-aac3-e063-6294a90a31b3 2025-02-12 Warnings Exact identifier application number: M003 Isopropyl alcohol 70 percent ISOPROPYL ALCOHOL Good Sense (Geiss, Destin & Dunn, Inc.) ac66be77-d358-44ea-8904-88186a7c2bbb 2025-02-07 Warnings Exact identifier application number: M003 Rubbing Alcohol 70 Percent Isopropyl ISOPROPYL ALCOHOL Harris Teeter, LLC 4196dd97-9041-4712-8196-02237a3b0cb2 2025-02-07 Warnings Exact identifier application number: M003 Isopropyl alcohol 91 percent ISOPROPYL ALCOHOL Harris Teeter, LLC 1b044f47-45e1-40a3-81b0-2717ed425f16 2025-02-07 Warnings Exact identifier application number: M003 Instant Hand Sanitizer ETHYL ALCOHOL Rejoice International Corp. 4e042f5b-3f0c-1830-e054-00144ff88e88 2025-02-06 Warnings Exact identifier application number: M003 Instant Hand Sanitizer ETHYL ALCOHOL Rejoice International Corp. 4e04fa70-c25d-4499-e054-00144ff8d46c 2025-02-06 Warnings Exact identifier application number: M003 Instant Hand Sanitizer ETHYL ALCOHOL Rejoice International Corp. 4e05cceb-b8f3-48f7-e054-00144ff88e88 2025-02-06 Warnings Exact identifier application number: M003 Hand Sanitizer 1.8 oz Antiseptic ETHYL ALCOHOL REJOICE INTERNATIONAL CORP. a0313f20-11dc-6c7d-e053-2a95a90a60f1 2025-02-06 Warnings Exact identifier application number: M003
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68062-2243-1 68062224301 120 mg in 1 BOTTLE (68062-2243-1) 120 mg 2020-09-17 0000-00-00 No No Current 68062-2243-2 68062224302 100 mg in 1 BOTTLE (68062-2243-2) 100 mg 2025-10-10 No No Current