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 |
|---|---|---|---|---|---|---|
| Walgreens Sanitizing Wipes | WALGREENS SANITIZING WIPES | Walgreens | 42de3b25-692b-eaff-e063-6294a90a0d21 | 2026-03-11 | Warnings | M003 |
| 70% Isopropyl Alcohol | ISOPROPYL ALCOHOL | Amazon.com Services LLC | 106f51fa-e687-470f-8ed8-35cb0565aeff | 2026-03-11 | Warnings, Adverse reactions | M003 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Amazon.com Services LLC | 4ab76d25-136d-45e2-b9d7-964777e1d855 | 2026-03-11 | Warnings, Adverse reactions | M003 |
| Hydrogen Peroxide | HYDROGEN PEROXIDE | Perrigo Direct, Inc | 2efcda54-b8b7-4266-89c0-7f686c7afdca | 2026-03-11 | Warnings, Adverse reactions | M003 |
| Alcohol Antiseptic Pads | ISOPROPYL ALCOHOL | Acme United Corporation | 4cc307b9-aee2-3ce0-e063-6294a90aa169 | 2026-03-11 | Warnings | M003 |
| Isopropyl alcohol | ISOPROPYL ALCOHOL | Salado Sales Inc. | 30294cad-d806-4d5b-8c86-484f22d214b6 | 2026-03-10 | Warnings, Adverse reactions | M003 |
| mild iodine tincture | IODINE AND SODIUM IODINE AND ALCOHOL | KROGER COMPANY | 42762471-e5cb-505e-e063-6294a90afb7d | 2026-03-10 | Warnings | M003 |
| Numstat Antiseptic and Pain-Relieving Prep Pad | ANTISEPTIC AND PAIN-RELIEVING PREP PAD | Safetec of America Inc. | 4c9c20f2-bc17-857b-e063-6394a90a5d5c | 2026-03-09 | Warnings | M003 |
| Eco Bandage OCEAN | BENZETHONIUM CHLORIDE | ECO Bandage LLC | c7867df0-e167-4ec6-921b-6a0fb3cb0614 | 2026-03-06 | Warnings | M003 |
| Eco Bandage HONEY | BENZETHONIUM CHLORIDE | Eco Bandage LLC | d2faa027-b274-43c0-9b87-85efab89fe8e | 2026-03-06 | Warnings | M003 |
| Eco Bandage HIBISCUS | BENZETHONIUM CHLORIDE | Eco Bandage LLC | 41f8716d-a970-40cd-a29d-69dafc97def8 | 2026-03-06 | Warnings | M003 |
| Eco Bandage MOCHA | BENZETHONIUM CHLORIDE | Eco Bandage LLC | 11ec42e4-49d1-4690-80c3-784f2e30acd3 | 2026-03-06 | Warnings | M003 |
| Eco Bandage SAND | BENZETHONIUM CHLORIDE | Eco Bandage LLC | 5c620696-e8eb-445e-b746-5348ea37a214 | 2026-03-06 | Warnings | M003 |
| Eco Bandage sand ocean | BENZETHONIUM CHLORIDE | Eco Bandage LLC | da0c2d07-bc2a-4e7c-af45-f921375b52e1 | 2026-03-06 | Warnings | M003 |
| MediChoice Antiseptic Isopropyl Alcohol Prep Pads | ISOPROPYL ALCOHOL | O&M HALYARD, INC. | 20b3694e-04c7-4bca-b2ce-62ae0dec7a83 | 2026-03-05 | Warnings | M003 |
| MediChoice Alcohol Swabstick | ISOPROPYL ALCOHOL | O&M HALYARD, INC. | 7f78529d-df17-44b3-a890-1afa35308c67 | 2026-03-05 | Warnings | M003 |
| MediChoice Alcohol Prep Pads | ISOPROPYL ALCOHOL | O&M HALYARD, INC. | f4f54448-0de0-448c-9b7b-104370953ae5 | 2026-03-05 | Warnings | M003 |
| MediChoice Alcohol Swabstick | ISOPROPYL ALCOHOL | O&M HALYARD, INC. | 7cee1141-4a49-4fec-a627-91a88e3d3ffc | 2026-03-05 | Warnings | M003 |
| Loris BZK Antiseptic Wipes | BENZALKONIUM CHLORIDE | LernaPharm Loris Inc. | a448de7b-4d96-4d53-ae1a-0bd38a2fb4a2 | 2026-03-05 | Warnings | M003 |
| SPA HAND SANITIZER WRTER MELON SPLASH | ETHYL ALCOHOL | Rejoice International Corp. | 4c53620d-01ee-8ddd-e063-6294a90a8a2b | 2026-03-05 | 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 |