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 |
|---|---|---|---|---|---|---|
| Coralite Capsaicin Heat Patch 2ct | CAPSAICIN | United Exchange Corp. | 4128b1ac-f540-2611-e063-6294a90ac98b | 2025-10-08 | Warnings | M017 |
| Ombre Men overtime wipes | BENZOCAINE | Sambria Pharmaceuticals, LLC | 405f23ca-99c1-4db4-aba1-2fd7f93f55ee | 2025-10-07 | Warnings | M017 |
| Pain free IV | LIDOCAINE | Sambria Pharmaceuticals, LLC | 7aa4cb20-d452-417f-afdb-307df754ed75 | 2025-10-07 | Warnings | M017 |
| HYDROCORTISONE | HYDROCORTISONE | CVS PHARMACY, INC | b3bdff5e-37fe-442a-a370-7b19799ea781 | 2025-10-07 | Warnings | M017 |
| HealthWise Pain Relief Patch | MENTHOL, METHYL SALICYLATE | Veridian Healthcare | b65932fd-ee9f-4fa2-b842-01e0f54133c9 | 2025-10-07 | Warnings | M017 |
| AREX SINSIN PAS | CAMPHOR, MENTHA OIL, MENTHOL, METHYL SALICYLATE, ZINC OXIDE | Sinsin Pharmaceutical Co., Ltd. | 2013ea44-e2ea-4b36-bddb-7f64163284b6 | 2025-10-07 | Warnings | M017 |
| SINSINPAS LIDOCAINE PAIN RELIEVING | LIDOCAINE | Sinsin Pharmaceutical Co., Ltd. | 82c0a036-8750-5b3d-e053-2a91aa0a1815 | 2025-10-07 | Warnings | M017 |
| SINSIN MULPAS | L-MENTHOL, METHYL SALICYLATE, DL-CAMPHOR, CHLORPHENIRAMINE MALEATE, THYMOL | Sinsin Pharmaceutical Co., Ltd. | 81baffcb-c08e-4616-e053-2a91aa0aaf15 | 2025-10-07 | Warnings | M017 |
| Arex Sinsin Pas | CAMPHOR, MENTHA OIL, MENTHOL, METHYL SALICYLATE, ZINC OXIDE | Sinsin Pharmaceutical Co., Ltd. | a851854a-5dfe-4bd5-95f6-67c3f13f1187 | 2025-10-07 | Warnings | M017 |
| Sinsinpas Arex Flex Gel Pain Relieving Patch | L-MENTHOL | Sinsin Pharmaceutical Co., Ltd. | 1758ef9b-4fac-4066-e063-6394a90a8cc3 | 2025-10-07 | Warnings | M017 |
| SINSINPAS CORN REMOVER | SALICYLIC ACID | Sinsin Pharmaceutical Co., Ltd. | e2771dfc-ee57-553f-e053-2a95a90af281 | 2025-10-07 | Warnings | M017 |
| Feminine Anti-Itch Creme | BENZOCAINE, RESORCINOL | Quality Choice (CHAIN DRUG MARKETING ASSOCIATION) | aa6cc963-dc60-5222-e053-2995a90acaf6 | 2025-10-06 | Warnings | M017 |
| TheraCare 2% Diphenhydramine Anti-Itch Cream | DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE | Veridian Healthcare | 5999b677-63dd-49c6-b5b8-7b3c117ecc5c | 2025-10-06 | Warnings | M017 |
| HealthWise Pain Relief | MENTHOL | Veridian Healthcare | 06be5331-7a1e-4ab3-9f17-2d350bd4b890 | 2025-10-02 | Warnings | M017 |
| equate Burn Relief | LIDOCAINE HYDROCHLORIDE | Walmart Inc | a90cbd92-80a5-4463-8152-b83165121a6f | 2025-10-02 | Warnings | M017 |
| AsperFlex HOT | CAMPHOR, MENTHOL, METHYL SALICYLATE | Akron Pharma Inc. | a6cb0656-8866-44ff-b40c-73655ff68721 | 2025-10-02 | Warnings | M017 |
| AsperFlex Original Maximum Strength | MENTHOL | Akron Pharma Inc. | d766c61e-c48b-4aff-97b0-678159479e03 | 2025-10-02 | Warnings | M017 |
| HealthWise Feminine Anti-Itch Cream | BENZOCAINE, RESORCINOL | Veridian Healthcare | 1f9110da-f448-8e20-e063-6294a90a4275 | 2025-10-02 | Warnings | M017 |
| PROSTAT FIRST AID Burn Ease, 0.9g | LIDOCAINE | ProStat First Aid LLC | dc704403-e2aa-47f7-a7f4-f6afe1547ca8 | 2025-10-01 | Warnings | M017 |
| PROSTAT FIRST AID Burn Ease, 0.9g | LIDOCAINE | ProStat First Aid LLC | e02558a9-fe2b-4f28-9fd3-7308f859d759 | 2025-10-01 | 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 |