Point Relief Cold Spot Pain Relieving
- Product NDC
- 51452-035
- 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 | 2026-10-20 | |
| excluded package | package | 51452-035 | 51452-035-04 | D | Discontinued by firm | 2026-10-20 |
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 | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | 51452-035-01 | d630ba8d3edf… | 732f749b63fb… |
| 2025-12-14 17:58 UTC · source 2025-12-05 | 51452-035-04 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | 51452-035-01 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | 51452-035-04 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 51452-035-01 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 51452-035-04 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | 51452-035-01 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | 51452-035-04 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | 51452-035-01 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | 51452-035-04 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | 51452-035-01 | cdf11ea48f46… | ba0047e9e063… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | 51452-035-04 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 51452-035-01 | 302b2466d912… | e7b80fea0513… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 51452-035-04 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | 51452-035-01 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | 51452-035-04 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 51452-035-01 | 0efc9e666f02… | f202fb6c5f17… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 51452-035-04 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | 51452-035-01 | ad56d346431e… | cc804d4bbf1e… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | 51452-035-04 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 51452-035-01 | 367a005e9d99… | 383a685ebd0f… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 51452-035-04 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 51452-035-01 | 557ba5c1ecfa… | 9c80585c8c6e… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 51452-035-04 | 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 |
|---|---|---|---|---|---|---|
| VBBV Tattoo Numbing | LIDOCAINE | Jiashen International Trade Limited | 3557859e-f8b3-1049-e063-6394a90ad737 | 2025-05-17 | Warnings | M017 |
| Bliss Republic Lidocaine Numbing Cream | LIDOCAINE NUMBING CREAM | Sargass Group Limited Liability Company | 35415851-beba-5bb4-e063-6294a90a35c0 | 2025-05-16 | Warnings | M017 |
| Cold Hot Chinese Red Tiger Pain Relief Gel Roll-On | MENTHOL | Guangzhou Zhupuyou E-commerce Co., Ltd | 352798e1-1e09-3d47-e063-6394a90ad404 | 2025-05-15 | Warnings | M017 |
| Plantar Fasciitis Chinese Red Tiger Pain Relief Gel Roll-On | MENTHOL | Guangzhou Zhupuyou E-commerce Co., Ltd | 35285d62-c660-a056-e063-6294a90aabc8 | 2025-05-15 | Warnings | M017 |
| SionBiotext Hydrocortisone | HYDROCORTISONE ACETATE 1% | Sion Biotext Medical Ltd | 35073eae-26fe-2bb5-e063-6294a90ab56a | 2025-05-13 | Warnings | M017 |
| Bliss Republic Lidocaine Numbing Cream | LIDOCAINE NUMBING CREAM | Sargass Group Limited Liability Company | 3508ae14-d9c9-3c85-e063-6294a90a0098 | 2025-05-13 | Warnings | M017 |
| SORE NO MORE WARM THERAPY | MENTHOL AND CAMPHOR | SOMBRA COSMETICS INC. | cd86b56e-9b4c-4aca-9740-c8793cb12055 | 2025-05-12 | Warnings | M017 |
| SORE NO MORE COOL THERAPY | MENTHOL | SOMBRA COSMETICS INC. | 9aa1f0ac-3baf-4e45-9e3a-c28a99b22909 | 2025-05-12 | Warnings | M017 |
| Calm and Correct Serum with Lidocaine | LIDOCAINE 3 PERCENT | Renu Laboratories, LLC | ddcf1c2e-2f67-44d7-e053-2a95a90a812b | 2025-05-09 | Warnings | M017 |
| Mqupin Knee Patch | KNEE PATCH | Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd | 09772e4b-8193-3771-e063-6394a90a9516 | 2025-05-08 | Warnings | M017 |
| Hydrocortisone Cream | HYDROCORTISONE | Trifecta Pharmaceuticals USA | d57a59fb-c8f2-f73b-e053-2995a90a4cdb | 2025-05-08 | Warnings | M017 |
| Hydrocortisone Cream | HYDROCORTISONE | Trifecta Pharmaceuticals USA | 4c96ec41-841c-322b-e054-00144ff8d46c | 2025-05-08 | Warnings | M017 |
| GNP Extra Strength Anti-Itch Cream | DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE | Amerisource Bergen | 34a66224-ef3c-e36e-e063-6394a90ac99d | 2025-05-08 | Warnings | M017 |
| Good Neighbor Muscle Rub Cream | CAMPHOR 4.0%, MENTHOL 10.0%, METHYL SALICYLATE 30.0%, | Amerisource Bergen | 34924bb9-e3e8-70e6-e063-6294a90aaa8c | 2025-05-07 | Warnings | M017 |
| DermaRad Relief Post Radiation Calming | LIDOCAINE 3 PERCENT | Renu Laboratories, LLC | e5d64929-fb9c-7ebc-e053-2995a90a9318 | 2025-05-07 | Warnings | M017 |
| Cold Hot Medicated Patch 5% Menthol | MENTHOL | InterMed Laboratories Private Limited | 33ee0235-5a6e-0ea1-e063-6394a90a89a5 | 2025-05-06 | Warnings | M017 |
| DermaRad Relief | LIDOCAINE EMULSION | RENU LABORATORIES, LLC | d5e11f73-918b-eeac-e053-2995a90a4a83 | 2025-05-06 | Warnings | M017 |
| Plantar Fasciitis Pain Relief Gel-Patch | LIDOCAINE, MENTHOL | Guangzhou Zhupuyou E-commerce Co., Ltd | 34838622-b092-afeb-e063-6294a90ae7db | 2025-05-06 | Warnings | M017 |
| Climax Shield Delay | BENZOCAINE | PRODUCT MAX GROUP INC | 9c720cdc-f753-47ce-95ff-3b26e461a0ab | 2025-05-05 | Warnings | M017 |
| PediFix Lidocaine Pain-Relief Patches | LIDOCAINE PAIN-RELIEF PATCHES | PediFix, Inc | 346550b9-d2ba-184e-e063-6394a90a591a | 2025-05-05 | 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 |
| 51452-035-02 | 51452003502 | 475 mL in 1 BOTTLE (51452-035-02) | 475 ml | 2019-04-01 | 0000-00-00 | No | No | Current |
| 51452-035-03 | 51452003503 | 3800 mL in 1 JUG (51452-035-03) | 3800 ml | 2019-04-01 | 0000-00-00 | No | No | Current |
| 51452-035-04 | 51452003504 | 420 mL in 1 TUBE (51452-035-04) | 420 ml | 2019-04-01 | 0000-00-00 | No | No | Current |
| 51452-035-05 | 51452003505 | 950 mL in 1 BOTTLE (51452-035-05) | 950 ml | 2019-04-01 | 0000-00-00 | No | No | Current |