MyDerm
- Product NDC
- 72667-008
- 11-digit product format
- 726670008
- Labeler code
- 72667
- Product ID
- 72667-008_37d85e33-0941-1973-e063-6394a90a3424
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lidocaine
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Inspec Solutions LLC.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-02-26
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- .5 g/100mL
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 72667-008 | D | Discontinued by firm | 2026-10-23 | ||
| excluded package | package | 72667-008 | 72667-008-08 | D | Discontinued by firm | 2026-10-23 | |
| excluded package | package | 72667-008 | 72667-008-09 | D | Discontinued by firm | 2026-10-23 |
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 | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 72667-008-01 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 72667-008-01 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 72667-008-01 | 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
- MyDerm
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| LIDOCAINE HYDROCHLORIDE | .5 g/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| V13007Z41A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1011849 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 82d075d1-c92e-2097-e053-2991aa0ab131 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 070fbed5-7088-434a-a7ce-f2a64d8d40ac | Product name | 2 | 20260107 |
| bee66ce1-adb7-9d3b-67d9-582e4c54e80f | Product name | 5 | 20250819 |
| 860a93dc-4863-49cc-b284-6bbe8191bc48 | Product name | 4 | 20250214 |
| eaba870a-6a9d-442e-8643-87b3f558a451 | Product name | 1 | 20250117 |
| 9b4cf230-fd05-41d5-98c6-5db9ecb27b86 | Product name | 1 | 20230117 |
| 7d755fa1-1087-4dcd-98f0-6d4bba479a57 | Product name | 3 | 20210602 |
| aed701d5-9c75-dfaf-7154-cde46179faea | Product name | 9 | 20200313 |
| fa8b5901-e681-426f-82fe-54f6d81ec698 | Product name | 4 | 20180619 |
| 332d03e4-aa24-4b11-841a-02bf41081920 | Product name | 1 | 20171221 |
| c08ab52f-2fc8-4409-9d9f-ed8edc0bd070 | Product name | 1 | 20171221 |
| 68ed98f8-24c2-44a0-944a-6d36e82ce25a | Product name | 1 | 20141222 |
| 1cd42bc2-a430-c72b-636d-991b235fbf80 | Product name | 1 | 20140508 |
| 49fa150c-f0de-cce7-3d9c-993ed81c5698 | Product name | 1 | 20140508 |
| 4d7ae718-ed00-bae8-2abe-9eaec1eef7ff | Product name | 1 | 20140508 |
| 9137811f-f279-8640-5aeb-99fa2145d64d | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| Effective | Related label |
|---|---|
| 2025-02-05 | MyDerm Pain Reliever Aloe Gel Lidocaine HCI 0.5% |
| 2025-01-30 | MyDerm Pain Reliever Aloe Gel Lidocaine HCI 0.5% |
| 2021-12-14 | MyDerm Pain Reliever Aloe Gel Lidocaine HCI 0.5% |
| 2021-01-29 | MyDerm Pain Reliever Aloe Gel Lidocaine HCI 0.5% |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72667-008-01 | MyDerm | 237 mL in 1 BOTTLE, PLASTIC | GEL | 237 | 5 | |
| 72667-008-02 | MyDerm | 592 mL in 1 BOTTLE, PLASTIC | GEL | 592 | 5 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Alocane Max | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products LLC | 0a35ac19-6883-a733-e063-6294a90ad22d | 2024-11-05 | Warnings | M017 |
| Alocane Plus | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products, Inc. | cfe8114b-df65-064b-e053-2a95a90a33f6 | 2024-11-05 | Warnings | M017 |
| Alocane Botanicals | LIDOCAINE HYDROCHLORIDE | Quest Products, LLC. | 02a8e5c7-56f4-eb0d-e063-6294a90a80cd | 2024-11-05 | Warnings | M017 |
| Alocane Emergency Burn Pads | LIDOCAINE HYDROCHLORIDE | Quest Products, Inc. | fe58bb89-7216-4121-afd3-d1438bdfbfa2 | 2024-11-05 | Warnings | M017 |
| Licefreee AfterLice | PRAMOXINE HCI | Tec Laboratories Inc. | 06c4cc42-a215-3949-e063-6394a90a665e | 2024-11-05 | Warnings | M017 |
| Antibacterial Lidocaine Wound Gel | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE | ASO LLC | cb9505b7-222d-3a24-e053-2a95a90a0b64 | 2024-11-05 | Warnings | M017 |
| TopCare Pain Relieving Analgesic | LIDOCAINE HYDROCHLORIDE | Topco Associates LLC | 6b4783e0-1987-4838-9e8c-b95426d62b28 | 2024-11-05 | Warnings | M017 |
| Eagle Green Balm | CAMPHOR MENTHOL | Borden Company (Private) Limited | 6f7a796b-a31c-0e60-e053-2a91aa0a022b | 2024-11-04 | Warnings | M017 |
| Muscular Balm | CAPSAICIN MENTHOL METHYL SALICYLATE | Borden Company (Private) Limited | ed79f14e-6b3d-4bf2-9c34-d019c1ba2582 | 2024-11-04 | Warnings | M017 |
| Hydrocortisone with Aloe | HYDROCORTISONE | A-S Medication Solutions | 3e0aed2b-fee1-4a0c-a3d2-72cd2b3008e3 | 2024-11-04 | Warnings | M017 |
| Walgreens Ice Blue Pain Relieving Topical Analgesic | MENTHOL, UNSPECIFIED FORM | Walgreen Company | 1c0ee442-ffd2-4f6c-aab2-f70e295378ad | 2024-11-04 | Warnings | M017 |
| Walgreen Cool n Heat Maximum Strength Pain Relieving | MENTHOL, UNSPECIFIED FORM | Walgreen Company | d5c79476-dde8-4a85-8878-bc2ac3a3d70b | 2024-11-04 | Warnings | M017 |
| LIDOCAINE | LIDOCAINE | STRATUS PHARMACEUTICALS INC | 87a4f559-a4f6-4b9f-98de-b55b073a11c6 | 2024-11-01 | Warnings | M017 |
| Walgreens Nerve Pain Relieving Topical Analgesic | LIDOCAINE HYDROCHLORIDE AND MENTHOL, UNSPECIFIED FORM | Walgreen Company | 83849eca-e02f-4b43-b3a7-b25e987e08a8 | 2024-10-31 | Warnings | M017 |
| Sanar Naturals Arnica White | CAMPHOR | Sanvall Enterprises, Inc | 192039a2-aed6-821b-e063-6394a90a7f29 | 2024-10-31 | Warnings | M017 |
| Sanar Naturals Arnica Reforzada | CAMPHOR | Sanvall Enterprises, Inc | 1921a4b1-cd36-195e-e063-6294a90a8793 | 2024-10-31 | Warnings | M017 |
| Sanar Naturals Arnica Pain Releiving Roll On with Camphor | CAMPHOR | Sanvall Enterprises, Inc | 173db0e2-611f-55b9-e063-6394a90ac987 | 2024-10-31 | Warnings | M017 |
| Sanar Naturals Camphor | CAMPHOR | Sanvall Enterprises, Inc | 1921e851-cf83-0bdb-e063-6294a90a357f | 2024-10-31 | Warnings | M017 |
| cortisone | HYDROCORTISONE | CVS Pharmacy | c766deac-d993-4e48-a5c3-4cfde7338dff | 2024-10-31 | Warnings | M017 |
| Walgreens Pain Relieving with Lavender Analgesic | LIDOCAINE HYDROCHLORIDE | Walgreen Company | 6c7b39c8-5b65-430a-a529-5b6b14adce18 | 2024-10-31 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1011849 | lidocaine HCl 0.5 % Topical Gel | PSN | 82d075d1-c92e-2097-e053-2991aa0ab131 | 5 |
| 1011849 | lidocaine hydrochloride 0.005 MG/MG Topical Gel | SCD | 82d075d1-c92e-2097-e053-2991aa0ab131 | 5 |
| 1011849 | lidocaine hydrochloride 0.5 % Topical Gel | SY | 82d075d1-c92e-2097-e053-2991aa0ab131 | 5 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 72667-008-01 | 72667000801 | 237 mL in 1 BOTTLE, PLASTIC (72667-008-01) | 237 ml | 2019-02-26 | 0000-00-00 | No | No | Current |
| 72667-008-02 | 72667000802 | 592 mL in 1 BOTTLE, PLASTIC (72667-008-02) | 592 ml | 2019-02-26 | No | No | Current |