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.
| 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 |
|---|---|
| BENZALKONIUM CHLORIDE | .46 mg/240mg |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| F5UM2KM3W7 | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| ab9e2c3c-d422-255e-e053-2a95a90a7a22 | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68062-2242-1 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-a4df-d83d-e063-dadaa90ab31f | Dr Lift Antibacterial Hand Wash |
DailyMed Package Descriptions#
| 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 | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Hand Sanitizer | ALCOHOL | Trifecta Pharmaceuticals USA | 0ba469a8-53f3-eb8e-e063-6294a90a1efc | 2026-03-04 | Warnings | M003 |
| Isopropyl alcohol 91 percent ReadyInCase | ISOPROPYL ALCOHOL | P & L Development, LLC | a6d2068f-705d-4341-b1c8-81e1b563ab9a | 2026-03-04 | Warnings | M003 |
| 50% Isopropyl Alcohol | ISOPROPYL ALCOHOL | Amazon.com Services LLC | 95e31119-8487-4bc9-b1c2-c43d32fc80ce | 2026-03-03 | Warnings, Adverse reactions | M003 |
| FOOTSPA PEDI | ALCOHOL | CHEMCO CORPORATION | 3886a958-d035-ed15-e063-6294a90af1b5 | 2026-03-03 | Warnings | M003 |
| Medicated Apricot Scrub | SALICYLIC ACID | Old East Main Co. | 7c9c430b-30d8-4642-85bd-d028a9aa748a | 2026-03-02 | Warnings, Adverse reactions | M003 |
| First Aid Antiseptic | POVIDONE-IODINE | Old East Main Co. | fb9bbb51-d131-42b4-94e6-b752595b1081 | 2026-03-02 | Warnings | M003 |
| Isopropyl | ISOPROPYL ALCOHOL | Old East Main Co. | ea6f3065-780e-4afc-a361-a2cb296ae4d5 | 2026-03-02 | Warnings, Adverse reactions | M003 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Old East Main Co. | 2a09f6c0-e9a6-4f48-bce1-6cf7345f2d87 | 2026-03-02 | Warnings, Adverse reactions | M003 |
| 70% | ISOPROPYL ALCOHOL | Old East Main Co. | 3e7a7f3e-3e99-4999-95c2-1603aca08e89 | 2026-03-02 | Warnings, Adverse reactions | M003 |
| 50% Rubbing | ISOPROPYL ALCOHOL | Old East Main Co. | 2b600254-2a70-4254-85fb-29b9adb56c9a | 2026-03-02 | Warnings, Adverse reactions | M003 |
| Hydrogen Peroxide | HYDROGEN PEROXIDE | Old East Main Co. | 3c823b47-2ab7-4002-9b6f-abf0a3176b44 | 2026-03-02 | Warnings, Adverse reactions | M003 |
| American Red Cross 6oz, 3% Hydrogen Peroxide | AMERICAN RED CROSS 6 OZ, 3% HYDROGEN PEROXIDE SPRAY | MY IMPORTS USA LLC | 29299c46-a929-0d92-e063-6294a90a4218 | 2026-03-02 | Warnings | M003 |
| Isopropyl alcohol 91 percent | ISOPROPYL ALCOHOL | TARGET Corporation | c49f46c5-f9b2-4045-a31d-63cb22210233 | 2026-03-02 | Warnings | M003 |
| Isopropyl alcohol 91 percent | ISOPROPYL ALCOHOL | Sam's West, Inc | a9d6778a-e5ad-4e02-9142-4a932540eda7 | 2026-03-02 | Warnings | M003 |
| Hydrogen Peroxide | HYDROGEN PEROXIDE | Chain Drug Marketing Association | 31e7063e-0ba1-434f-b404-0ec42df634a3 | 2026-02-27 | Warnings, Adverse reactions | M003 |
| Iodine Tincture | IODINE TINCTURE | The Kroger Co. | c70a718f-d51a-455a-9785-ab41c1b1f8b0 | 2026-02-27 | Warnings, Adverse reactions | M003 |
| MedPride Sterile | BENZALKONIUM CHLORIDE | Shield Line LLC | 02f63d50-e4ff-49b6-9f8c-fddceefe65f3 | 2026-02-27 | Warnings | M003 |
| First Aid Antiseptic | POVIDONE-IODINE | Walmart Inc. | c8fa5ed3-0497-4a23-934b-c72ff02c94ae | 2026-02-27 | Warnings, Adverse reactions | M003 |
| FIGS - evolvetogether Hand Sanitizer FIGS 01 Ginger - Cedar Scented | ETHYL ALCOHOL | WE EVOLVETOGETHER INC. | 4bd5a36d-06b4-ba41-e063-6294a90aa121 | 2026-02-27 | Warnings | M003 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | United Natural Foods, Inc. dba UNFI | 4eee73dd-039e-44a5-b380-21ff32efee22 | 2026-02-26 | Warnings, Adverse reactions | M003 |
Packages#
| 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 |