MENTHOL
- Product NDC
- 72937-004
- 11-digit product format
- 729370004
- Labeler code
- 72937
- Product ID
- 72937-004_44141d2a-1d91-b970-e063-6294a90a53f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- SUNSET PAIN RELIEF ROLL-ON 3OZ
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-09-24
- Marketing end
- 2026-10-23
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 4 g/100mL
- NDC exclude flag
- No
- 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 package | package | 72937-004 | 72937-004-03 | D | Discontinued by firm | 2026-10-23 |
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
- MENTHOL
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MENTHOL, UNSPECIFIED FORM | 4 g/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| L7T10EIP3A | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 934d4638-b47b-187d-e053-2995a90ae69d | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 4d7a96d5-8256-4268-9a6c-25ea66d321fe | Product name | 1 | 20180814 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72937-004-03 | MENTHOL | 90 mL in 1 BOTTLE, WITH APPLICATOR | GEL | 90 | 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 |
|---|---|---|---|---|---|---|
| Lidocaine-Pain-Relief-Patch | LIDOCAINE-PAIN-RELIEF-PATCH | Henan Enokon Medical Instrument Co., Ltd. | 3ecfa867-50f6-d98a-e063-6394a90aefa0 | 2025-09-14 | Warnings | M017 |
| Meijer Hydrocortsione Cream | HYDROCORTSIONE CREAM 1% | Meijer Distribution Inc. | 1cbddb7e-f2e3-0951-e063-6394a90a3d37 | 2025-09-12 | Warnings | M017 |
| JO Prolonger with Benzocaine | BENZOCAINE | CC Wellness LLC | d955f612-1267-f1be-e053-2995a90a5345 | 2025-09-12 | Warnings | M017 |
| JO for Him Prolonger with Lidocaine | LIDOCAINE | CC Wellness LLC | b12dc6a3-142d-3219-e053-2995a90aead0 | 2025-09-12 | Warnings | M017 |
| Walgreens Medicated Foot Powder | MENTHOL | Davion, Inc | 58e1e7f7-6284-411f-9765-0e63eabca0f3 | 2025-09-12 | Warnings | M017 |
| PAIN RELIEF PATCHES | LIDOCAINE | Amerisource Bergen | 614f1e56-891f-4620-be10-0c075a1dbc3f | 2025-09-11 | Warnings | M017 |
| Industrial Itch and Pain Relief | DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE | R & R Lotion, Inc | 236415fc-f923-4a82-b54a-ecaf666dd2e0 | 2025-09-11 | Warnings | M017 |
| Eco Lips Menthol Medicated Lip Balm | MENTHOL | Eco Lips, Inc. | fc4c25d6-6109-dfd8-e053-6394a90a4e91 | 2025-09-10 | Warnings | M017 |
| Hydrocortisone | HYDROCORTISONE 1% | Encube Ethicals, Inc. | d6f5c0df-6262-4704-bb24-430f66bb2ca8 | 2025-09-09 | Warnings | M017 |
| Blue-Emu Lidocaine Pain Relief Cream | LIDOCAINE CREAM 4% | Kingsway Pharmaceuticals dba NFI, LLC | 592811f2-e21c-6a58-e053-2991aa0a69a9 | 2025-09-09 | Warnings | M017 |
| Hydrocortisone | HYDROCORTISONE | Unifirst First Aid Corporation | 282ed5ef-8c2a-4092-9d99-1a7eee7a39e3 | 2025-09-09 | Warnings | M017 |
| LubeLife Climax Control Delay | BENZOCAINE | CC Wellness LLC | e1a98e6d-0c24-75b8-e053-2a95a90ad136 | 2025-09-09 | Warnings | M017 |
| Blue-Emu Maximum Pain Relief | TROLAMINE SALICYLATE | Kingsway Pharmaceuticals dba NFI, LLC | c863351a-951b-4f7c-a9c0-4289d702054a | 2025-09-09 | Warnings | M017 |
| Tiger Balm Neck and Shoulder Rub | CAMPHOR (SYNTHETIC) AND MENTHOL | Haw Par Healthcare Ltd. | 02a65b25-78b2-4e29-9484-40e2228fb384 | 2025-09-09 | Warnings | M017 |
| Hydrocortisone | HYDROCORTISONE | Unifirst First Aid Corporation | e90df2e5-2ef4-47dd-bd74-be9cea6d9d85 | 2025-09-08 | Warnings | M017 |
| Hydrocortisone | HYDROCORTISONE | Unifirst First Aid Corporation | 69d6645e-db3c-4dc0-a9a5-e2bc963e2f28 | 2025-09-08 | Warnings | M017 |
| SupreH Arnica Bruise Cream | SUPREH ARNICA REMEDY PLUS BRUISE CREAM | Shenzhen Xinxin Yunhai Technology Co., Ltd. | 3e41fc0e-54c3-2622-e063-6294a90a13c9 | 2025-09-07 | Warnings | M017 |
| Menthol | MENTHOL | FlexiGo Inc | 3607c326-6db0-a2cd-e063-6394a90a9eb6 | 2025-09-06 | Warnings | M017 |
| TIDL PAIN RELIEF CRYOTHERAPY MENTHOL Cream | PAIN RELIEF CRYOTHERAPY MENTHOL CREAM | Shenzhen Sam Technology Co., Ltd. | 3e08cc87-2385-0838-e063-6394a90abf9b | 2025-09-05 | Warnings | M017 |
| TIDL CLINICAL CRYOTHERAPY MENTHOL Cream | CLINICAL CRYOTHERAPY MENTHOL CREAM | Shenzhen Sam Technology Co., Ltd. | 3e090b98-1db7-4174-e063-6394a90aa539 | 2025-09-05 | Warnings | M017 |
Packages#
| Package NDC | 11-digit format | Description | Units | Status |
|---|---|---|---|---|
| 72937-004-03 | 72937000403 | 90 mL in 1 BOTTLE, WITH APPLICATOR | 90 ml | Historical |