Point Relief Cold Spot Pain Relieving
- Product NDC
- 51452-035
- Requested package NDC
- 51452-035-01
- 11-digit product format
- 514520035
- Labeler code
- 51452
- Product ID
- 51452-035_0fc4ec9e-6c21-5a8c-e063-6394a90a11ef
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Fabrication Enterprises
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-04-01
- Substance
- MENTHOL
- Active strength
- 120 mg/mL
- 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 package | package | 51452-035 | 51452-035-01 | 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 | Snapshot | Source SHA-256 |
|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 557ba5c1ecfa… | 9c80585c8c6e… |
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
- Point Relief Cold Spot Pain Relieving
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MENTHOL | 120 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| L7T10EIP3A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2121666 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| ad5d6f04-15e6-4548-95c2-32271c186bc1 | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51452-035-01 | Point Relief Cold Spot Pain Relieving | 120 mL in 1 BOTTLE | GEL | 120 | 4 | |
| 51452-035-02 | Point Relief Cold Spot Pain Relieving | 475 mL in 1 BOTTLE | GEL | 475 | 4 | |
| 51452-035-03 | Point Relief Cold Spot Pain Relieving | 3800 mL in 1 JUG | GEL | 3800 | 4 | |
| 51452-035-04 | Point Relief Cold Spot Pain Relieving | 420 mL in 1 TUBE | GEL | 420 | 4 | |
| 51452-035-05 | Point Relief Cold Spot Pain Relieving | 950 mL in 1 BOTTLE | GEL | 950 | 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 |
|---|---|---|---|---|---|---|
| Overtime | METHYL SALICYLATE, MENTHOL AND CAPSAICIN | Physicians Science & Nature Inc. | 25fec070-8587-42d1-ba6f-1a9c150acc98 | 2025-11-10 | Warnings | M017 |
| Dendracin Neurodendraxcin | METHYL SALICYLATE, MENTHOL AND CAPSAICIN | Physicians Science & Nature Inc. | 05742cd5-ece2-4007-bdf0-46b76d23df74 | 2025-11-10 | Warnings | M017 |
| Anal Blu | DESENSITIZER | Novelties by Nasswalk, Inc. | 03b9555b-c3ff-4baa-e063-6394a90afb2c | 2025-11-10 | Warnings | M017 |
| Stallion | DELAY CREME | Novelties by Nasswalk, Inc. | 0261ec88-8fe4-d5f8-e063-6294a90ab3d4 | 2025-11-10 | Warnings | M017 |
| ANAL-ESE | DESENSITIZER | Novelties by Nasswalk, Inc. | 03b89eed-b433-a263-e063-6294a90a675b | 2025-11-10 | Warnings | M017 |
| Instant Erection | ULTIMATE ERECTION ENHANCER | Novelties by Nasswalk, Inc. | 03a444f9-7052-0c38-e063-6294a90a4e56 | 2025-11-10 | Warnings | M017 |
| STA-HARD | DESENSITIZING LUBRICANT | Novelties by Nasswalk, Inc. | 02ef794b-8e70-5c26-e063-6294a90a28d1 | 2025-11-10 | Warnings | M017 |
| ANAL-ESE | DESENSITIZER | Novelties by Nasswalk, Inc. | 03a4a7ce-4cff-a608-e063-6294a90ad65d | 2025-11-10 | Warnings | M017 |
| FOOTSPA PEDI | ALCOHOL | CHEMCO CORPORATION | 04de4392-74f6-7df8-e063-6294a90ae3b1 | 2025-11-08 | Warnings | M017 |
| Johnson and Johnson All Purpose First Aid Kit | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | 5cdb47c5-7951-4279-8a05-0a3199d3dd45 | 2025-11-06 | Warnings | M017 |
| Johnson and Johnson First Aid Travel Ready 80 CT | ACETAMINOPHEN, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | f388f105-48ba-4616-e053-2a95a90a0049 | 2025-11-06 | Warnings | M017 |
| Johnson and Johnson First Aid All Purpose 160 CT | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | f3933330-2550-4a88-e053-2a95a90a3997 | 2025-11-06 | Warnings | M017 |
| Foot and Leg Pain Relief | LIDOCAINE | Premier Brands of America Inc. | 42f23e2f-11c6-da49-e063-6294a90ac720 | 2025-11-06 | Warnings | M017 |
| HEALING TREE CALMING ANTI-ITCH | HYDROCORTISONE | Renu Laboratories, LLC | fc8bcde9-26e8-a35f-e053-6394a90a3300 | 2025-11-06 | Warnings | M017 |
| Calamine Plus | CALAMINE PLUS PRAMOXINE HCL | Chain Drug Marketing Association Inc | 1a3f8819-58cf-8923-e063-6394a90a37af | 2025-11-06 | Warnings | M017 |
| Extra Strength Itch Relief | DIPHENHYDRAMINE HCL AND ZINC ACETATE | Chain Drug Marketing Association Inc | 1a2997bc-7741-e658-e063-6394a90af6fd | 2025-11-06 | Warnings | M017 |
| Diphenhydramine HCl and Zinc Acetate | EXTRA STRENGTH ITCH RELIEF CONTINUOUS SPRAY | Topco Associates LLC | 8026c7dd-eb7b-ebea-e053-2991aa0a1b0f | 2025-11-06 | Warnings | M017 |
| Diphenhydramine HCl and Zinc Acetate | EXTRA STRENGTH ITCH RELIEF | Walgreen Company | 6057b4ff-6adc-4688-893c-62d237d7d1ae | 2025-11-06 | Warnings | M017 |
| BANPINGHUA Glucosamine Chondroitin Patch | PEPPERMINT, CAMPHOR, BORNEOL | Henan Lijitang Medical Technology Co., Ltd. | 42f8c2ae-50a2-2358-e063-6394a90a5979 | 2025-11-06 | Warnings | M017 |
| PAINGEL | CAMPHOR, MENTHOL | NACOR BUSINESS GROUP LLC | 42fa2397-b61a-3b16-e063-6294a90a5fed | 2025-11-06 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 2121666 | menthol 0.12 MG/MG Topical Gel | PSN | ad5d6f04-15e6-4548-95c2-32271c186bc1 | 4 |
| 2121666 | menthol 0.12 MG/MG Topical Gel | SCD | ad5d6f04-15e6-4548-95c2-32271c186bc1 | 4 |
| 2121666 | menthol 12 % Topical Gel | SY | ad5d6f04-15e6-4548-95c2-32271c186bc1 | 4 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 51452-035-01 | 51452003501 | 120 mL in 1 BOTTLE (51452-035-01) | 120 ml | 2019-04-01 | 0000-00-00 | No | No | Current |