CANNA NUMB Roll On
- Product NDC
- 72614-265
- 11-digit product format
- 726140265
- Labeler code
- 72614
- Product ID
- 72614-265_2e551eb2-3d15-0d28-e063-6394a90a4d9f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LIDOCAINE HYDROCHLORIDE, MENTHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Cannanumb LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-10-01
- Substance
- LIDOCAINE HYDROCHLORIDE; MENTHOL
- Active strength
- 40; 10 mg/mL; mg/mL
- 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
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
- CANNA NUMB Roll On
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| LIDOCAINE HYDROCHLORIDE | 40 mg/mL |
| MENTHOL | 10 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| V13007Z41A | Internal UNII lookup |
| L7T10EIP3A | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| c1eb0348-3b0e-4f1c-a46b-1ff4aa165fb4 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 860a93dc-4863-49cc-b284-6bbe8191bc48 | Product name | 4 | 20250214 |
| 9b4cf230-fd05-41d5-98c6-5db9ecb27b86 | Product name | 1 | 20230117 |
| 68ed98f8-24c2-44a0-944a-6d36e82ce25a | Product name | 1 | 20141222 |
| 1cd42bc2-a430-c72b-636d-991b235fbf80 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72614-265-02 | CANNA NUMB Roll On | 73 mL in 1 CONTAINER | LIQUID | 73 | 4 |
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 |
|---|---|---|---|---|---|---|
| Up up | PAIN RELIEF ADVANCED HYDROGEL PATCHES | Target Corporation | 44128b70-3172-ee37-e063-6294a90a705f | 2025-11-20 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET NOVELTIES, INC | f03090fa-f7e6-f53a-e053-2a95a90aa819 | 2025-11-20 | Warnings | M017 |
| HEATING PAIN RELIEF | METHYL SALICYLATE, MENTHOL | SUNSET NOVELTIES, INC | ff073e47-3107-e17e-e053-6294a90a58fa | 2025-11-20 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET NOVELTIES, INC | fc8a8f20-97ab-481e-e053-6394a90a3525 | 2025-11-20 | Warnings | M017 |
| MENTHOL | MENTHOL | SUNSET PAIN RELIEF ROLL-ON 3OZ | 934d4638-b47b-187d-e053-2995a90ae69d | 2025-11-20 | Warnings | M017 |
| FOOT PAIN RELIEF ROLL-ON | LIDOCAINE, MENTHOL | Guangzhou Zhupuyou E-commerce Co., Ltd | 43edcea0-ab04-f368-e063-6294a90a817a | 2025-11-19 | Warnings | M017 |
| Absolut Skin Corticosoothe Anti-Itch | HYDROCORTISONE | Absolut Skin Incorporated | deb52218-9176-4aaa-a22f-b66dada6690f | 2025-11-19 | Warnings | M017 |
| Maximum Strength 4% Lidocaine Patch Good Neighbor Pharmacy | LIDOCAINE | InterMed Laboratories Private Limited | 43f3d189-f6b7-02ed-e063-6394a90afd73 | 2025-11-19 | Warnings | M017 |
| Maximum Strength 4% Lidocaine Patch HealthA2Z | LIDOCAINE | InterMed Laboratories Private Limited | 43f3e288-e828-8130-e063-6394a90a6d44 | 2025-11-19 | Warnings | M017 |
| Maximum Strength 4% Lidocaine Patch Leader | LIDOCAINE | InterMed Laboratories Private Limited | 42f06914-c8b8-ea9c-e063-6294a90a79e6 | 2025-11-19 | Warnings | M017 |
| CVS Anti-Itch | CAMPHOR, MENTHOL | CVS | 87715662-c788-9a8d-e053-2a95a90acb53 | 2025-11-19 | Warnings | M017 |
| Walgreen Anti Itch | CAMPHOR, MENTHOL | Walgreens | b4f47a8d-d4a6-9233-e053-2a95a90afd90 | 2025-11-19 | Warnings | M017 |
| Leader Anti-Itch | CAMPHOR, MENTHOL | LEADER/Cardinal Helath 110, Inc. | 9ca985c6-5017-0558-e053-2995a90a8202 | 2025-11-19 | Warnings | M017 |
| CVS Anti-Itch | PRAMOXINE HCL | CVS | 87fc476a-5b12-7383-e053-2995a90a530b | 2025-11-19 | Warnings | M017 |
| Walgreen Anti-Itch | PRAMOXINE HCL | Walgreens | b5f9d1c5-891e-4377-e053-2995a90aa281 | 2025-11-19 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET PAIN RELIEF | 89f5f688-856f-f2df-e053-2995a90a73cf | 2025-11-19 | Warnings | M017 |
| Itch Eraser | DIPHENHYDRAMINE HCL | Tender Corporation d/b/a Adventure Ready Brands | 2204e135-6a23-68a2-e063-6394a90ac019 | 2025-11-18 | Warnings | M017 |
| Analgesic Balm | MENTHOL 10%, METHYL SALICYLATE 15% | Geri-Care Pharmaceuticals, Corp | c8594e10-661f-6ff3-e053-2995a90ab4fc | 2025-11-18 | Warnings | M017 |
| Mag 5 PT Cooling Formula Recovery Cream | MENTHOL | RENU LABORATORIES, LLC | a45cde67-64ec-643b-e053-2a95a90a10b6 | 2025-11-18 | Warnings | M017 |
| After Ivy Wipe | CAMPHOR | Tender Corporation d/b/a Adventure Ready Brands | 21d98018-826a-1d0d-e063-6294a90a0a71 | 2025-11-17 | Warnings | M017 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 72614-265-02 | 72614026502 | 73 mL in 1 CONTAINER (72614-265-02) | 73 ml | 2018-10-01 | 0000-00-00 | No | No | Current |