Dr Lift Antibacterial Body Scrub
- Product NDC
- 68062-2240
- 11-digit product format
- 680622240
- Labeler code
- 68062
- Product ID
- 68062-2240_50b7202c-ebc3-d203-e063-6394a90ac911
- 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
- .23 mg/180mg
- 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 | 68062-2240-1 | 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 | 68062-2240-1 | 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 | 68062-2240-1 | 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 | 68062-2240-1 | 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 | 68062-2240-1 | 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 | 68062-2240-1 | 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 | 68062-2240-1 | 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 | 68062-2240-1 | 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 | 68062-2240-1 | 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 Body Scrub
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZALKONIUM CHLORIDE | .23 mg/180mg |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| F5UM2KM3W7 | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| ab9d6c73-29c1-036a-e053-2995a90a449c | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68062-2240-1 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-6b42-d83d-e063-dadaa90ab31f | Dr Lift Antibacterial Body Scrub |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68062-2240-1 | Dr Lift Antibacterial Body Scrub | 180 mg in 1 TUBE | GEL | 180 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68062-2240 | DR LIFT ANTIBACTERIAL BODY SCRUB (BENZALKONIUM CHLORIDE) GEL [SPA DE SOLEIL] | 1 | Current NDC, Legacy NDC, 1 package rows | 20200730_ab9d6c73-29c1-036a-e053-2995a90a449c.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 |
|---|---|---|---|---|---|---|
| Alcohol sterile | ISOPROPYL ALCOHOL | Cardinal Health, Inc | bb7c530f-5d80-4158-b715-09c1c837299d | 2024-11-21 | Warnings | M003 |
| Alcohol sterile | ISOPROPYL ALCOHOL | Cardinal Health 200 LLC | 10135db9-f614-4511-96ac-faa6a02a1b61 | 2024-11-21 | Warnings | M003 |
| BZK Antiseptic Swabsticks 4 Triple | BENZALKONIUM CHLORIDE | Changzhou Maokang Medical Products Co., Ltd | d9f35c14-2f5a-4e1a-bc2b-a7e163134213 | 2024-11-21 | Warnings | M003 |
| Povidone-lodine Swabsticks Triple | POVIDONE-IODINE | Changzhou Maokang Medical Products Co., Ltd | 74e70ea9-640b-4295-a40f-56f65fca1300 | 2024-11-21 | Warnings | M003 |
| MK Alcohol Prep Pads Medium | ISOPROPYL ALCOHOL | Changzhou Maokang Medical Products Co., Ltd | 37f10b1f-b73c-4d71-91c2-1252f3d9d4ce | 2024-11-21 | Warnings | M003 |
| BZK Antiseptic Towelette | BENZALKONIUM CHLORIDE | Changzhou Maokang Medical Products Co., Ltd | 1936d749-bf38-a433-e063-6294a90aba8c | 2024-11-21 | Warnings | M003 |
| Maokang 10 Povidone Iodine | POVIDONE-IODINE | Changzhou Maokang Medical Products Co., Ltd | 7c17ce40-0358-44ff-aa60-53711666914b | 2024-11-21 | Warnings | M003 |
| MK Alcohol Prep Pads Medium | ISOPROPYL ALCOHOL | Changzhou Maokang Medical Products Co., Ltd | 11390854-9e72-40a2-9c89-3c29a585dced | 2024-11-21 | Warnings | M003 |
| Instant Hand Sanitizeing Wipe | ISOPROPANOL AND COMPOUND DOUBLE-STRANDED QUATERNARY AMMONIUM SALTS | Shandong Yayun Sanitary Products Co., Ltd. | aa0dc01a-2c6b-7402-e053-2a95a90af6a2 | 2024-11-21 | Warnings | M003 |
| Dynarex Povidone Iodine Prep Solution | POVIDONE IODINE PREP SOLUTION | Dynarex Corporation | 6bb4d55b-2be7-3549-e053-2a91aa0a2bb0 | 2024-11-20 | Warnings | M003 |
| Dynarex Povidone Iodine Surgical Scrub | POVIDONE IODINE SURGICAL SCRUB SOLUTION | Dynarex Corporation | 6f053e55-cbf6-9072-e053-2991aa0a2edd | 2024-11-20 | Warnings | M003 |
| Dynarex Green | ALCOHOL | Dynarex Corporation | 072572be-49dd-4594-bc40-b56db57ada5b | 2024-11-20 | Warnings | M003 |
| Dynarex Green | CHLOROXYLENOL | Dynarex Corporation | 59b098d2-08de-4fdb-a209-ae226abf37d6 | 2024-11-20 | Warnings | M003 |
| Baby Wipes | PROPYLENE GLYCOL | Shandong Yayun Sanitary Products Co., Ltd. | aeb9a12c-955f-5030-e053-2995a90a2dd6 | 2024-11-20 | Warnings | M003 |
| Pet wipes | BENZALKONIUM CHLORIDE | Shandong Yayun Sanitary Products Co., Ltd. | 2764ea79-32d8-b7f6-e063-6394a90a5501 | 2024-11-20 | Warnings | M003 |
| Premium Hand Sanitizer | ETHANOL | MCKESSON MEDICAL-SURGICAL INC. | a9514466-e0c6-4792-984a-9f07d94ee887 | 2024-11-18 | Warnings | M003 |
| MARVEL BZK ANTISEPTIC WIPE | BENZALKONIUM CHLORIDE | Ashtel Studios, Inc. | 93ed0bb4-834d-44ca-9c0a-20086fc09ab8 | 2024-11-18 | Warnings | M003 |
| Isopropyl Rubbing Alcohol | ISOPROPYL ALCOHOL | McKesson Medical-Surgical Inc. | 98b0bcc2-539b-4471-ba98-bbe17bb881bd | 2024-11-15 | Warnings | M003 |
| CVS Health Hydrogen Peroxide Wipes | HYDROGEN PEROXIDE | CVS PHARMACY, INC | 7a930a5e-5b69-428f-9cbb-d03dae180295 | 2024-11-12 | Warnings | M003 |
| First Aid Only Povidone-Iodine Prep Pad | POVIDONE-IODINE | Acme United Corporation | 509b6c8e-6a9f-2656-e054-00144ff8d46c | 2024-11-09 | Warnings | M003 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 68062-2240-1 | 68062224001 | 180 mg in 1 TUBE (68062-2240-1) | 180 mg | 2020-07-29 | 0000-00-00 | No | No | Current |