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 |
|---|---|---|---|---|---|---|
| Family Care Anti-Itch | HYDROCORTISONE | United Exchange Corp. | 8e4d46d8-7084-0666-e053-2995a90ad520 | 2025-10-21 | Warnings | M017 |
| Coralite Pain Relief | CAMPHOR, MENTHOL, METHYL SALICYLATE | United Exchange Corp. | 69aec845-3d4c-d226-e053-2991aa0afd12 | 2025-10-21 | Warnings | M017 |
| WHITE FLOWER ANALGESIC BALM | CAMPHOR, MENTHOL AND METHYL SALICYLATE | HOE HIN PAK FAH YEOW MANUFACTORY LTD | f3e3b8b5-b12b-49ac-9318-b0c358b136e9 | 2025-10-21 | Warnings | M017 |
| Mountain Ice Sports Recovery | MENTHOL | Mountainside Medical Equipment, Inc. | 98638529-3c17-436e-901f-c8aea52bdab6 | 2025-10-20 | Warnings | M017 |
| Lip Clear Lysine Plus | MENTHOL, UNSPECIFIED FORM | Quantum, Inc. | 21a5b4fb-baed-4766-9820-5c6051c14720 | 2025-10-20 | Warnings | M017 |
| Buzz Away Sting Soothe | MENTHOL | Quantum, Inc. | 419e34ea-17b2-ec32-e063-6394a90a603d | 2025-10-20 | Warnings | M017 |
| Family Care Anti-Itch | HYDROCORTISONE | United Exchange Corp. | deb09e89-9794-89a7-e053-2a95a90abdf8 | 2025-10-20 | Warnings | M017 |
| Numbing Cream | MENTHOL | FlexiGo Inc | 41571c8f-332b-f423-e063-6394a90a8897 | 2025-10-20 | Warnings | M017 |
| Soothing Nerve Therapy | MENTHOL | Wise Consumer Products | 40829d6b-5005-7ec9-e063-6294a90a970e | 2025-10-20 | Warnings | M017 |
| Numbing Cream | MENTHOL | FlexiGo Inc | 4146fd51-b18c-393d-e063-6294a90a4d9a | 2025-10-20 | Warnings | M017 |
| Lidocaine 4% Maximum OTC Strength | LIDOCAINE | Cardinal Health 107, LLC | 975031df-d46d-4098-b1c0-1c0c92b41995 | 2025-10-20 | Warnings | M017 |
| Cortizone 10 Intensive Healing | HYDROCORTISONE | Chattem, Inc. | bb3d1a3e-4c0c-4694-9c05-80152dd9bd1c | 2025-10-20 | Warnings | M017 |
| Sting relief pad | BENZOCAINE, ALCOHOL | Guangdong Comfort Medical Products Co., Ltd. | 6e905065-10a9-1ded-e053-2a91aa0a46a1 | 2025-10-19 | Warnings | M017 |
| CVS Cold and Hot | MENTHOL | CVS Pharmacy | a44cec95-822a-40b6-e053-2995a90ae31c | 2025-10-17 | Warnings | M017 |
| Sombra Max | SOMBRA MAX | Sombra Cosmetics Inc. | 41623a46-e6e7-907e-e063-6394a90afc4c | 2025-10-17 | Warnings | M017 |
| POMADA DRAGON PAIN RELIEVING | CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE | TELEVISA CONSUMER PRODUCTS USA | c283291d-feaa-4f89-8fde-9e3957ea8b9f | 2025-10-17 | Warnings | M017 |
| Ear Pain MD | LIDOCAINE HYDROCHLORIDE | Eosera Inc | 78c4418f-7f0f-447f-a94f-d4c89a081af1 | 2025-10-17 | Warnings | M017 |
| WOFANLI Quit Smoking Nicotine Patches | NICOTINE TRANSDERMAL PATCHES | Shenzhen Paxi Trading Co., Ltd. | 414217c1-ff3a-b556-e063-6394a90aa5db | 2025-10-16 | Warnings | M017 |
| WOFANLI Quit Smoking Nicotine Patches | NICOTINE TRANSDERMAL PATCHES | Shenzhen Paxi Trading Co., Ltd. | 41422d04-160b-51b2-e063-6294a90ab2b2 | 2025-10-16 | Warnings | M017 |
| WOFANLI Quit Smoking Nicotine Patches | NICOTINE TRANSDERMAL PATCHES | Shenzhen Paxi Trading Co., Ltd. | 41427275-4c35-bbdf-e063-6294a90a14cf | 2025-10-16 | 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 |