NDC 52000-072-01 - Muscle Rub Pain Reliever Gel
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 52000-072
- Requested NDC
- 52000-072-01
- Package NDCs from labels
- 52000-072-03, 52000-072-04, 52000-072-01, 52000-072-02
- Manufacturer
- Universal Distribution Centre LLC
- Effective date
- 2025-10-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Muscle Rub Pain Reliever Gel - Universal Distribution Centre LLC | Universal Distribution Centre LLC | 2025-10-30 | HUMAN OTC DRUG LABEL |
| Muscle Rub Pain Reliever Gel - Universal Distribution Centre LLC | Universal Distribution Centre LLC | 2024-12-03 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 52000-072-02 | 2025-07-29 | C162847 | 48780-1 | 3b156c62-308b-fb37-e063-e6dba90a4e07 | Pain Reliever Gel |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52000-072-01 | Muscle Rub Pain Reliever Gel | 35.4 g in 1 TUBE | GEL | 35.4 | 4 | |
| 52000-072-02 | Muscle Rub Pain Reliever Gel | 1 in 1 CARTON | GEL | 1 | 4 | |
| 52000-072-03 | Muscle Rub Pain Reliever Gel | 35.4 g in 1 TUBE | GEL | 35.4 | 3 | |
| 52000-072-04 | Muscle Rub Pain Reliever Gel | 1 in 1 CARTON | GEL | 1 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 52000-072 | MUSCLE RUB PAIN RELIEVER GEL (MENTHOL, UNSPECIFIED FORM) GEL [UNIVERSAL DISTRIBUTION CENTRE LLC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20241212_b9a563b6-7988-79df-e053-2995a90a752b.zip |
| 52000-072 | MUSCLE RUB PAIN RELIEVER GEL (MENTHOL, UNSPECIFIED FORM) GEL [UNIVERSAL DISTRIBUTION CENTRE LLC] | 2 | Current NDC, Legacy NDC, 2 package rows | 20241218_18536e21-afc3-8447-e063-6394a90aabae.zip |
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 |
|---|---|---|---|---|---|---|
| JenGufun LIDOCAINE KNEE Patch | LIDOCAINE KNEE PATCH | Henan Kangdi Medical Devices Co., Ltd. | 5b1d8508-b993-7a8d-e063-6294a90ae306 | 2026-09-10 | Warnings | M017 |
| OTTFFSS SMELLING SALTS | MENTHOL 15% SMELLING SALTS | Hubei Minxin Pharmaceutical Co., Ltd. | 5b0991b6-59cc-59b3-e063-6394a90a7693 | 2026-09-09 | Warnings | L7T10EIP3A |
| THITFAM SMELLING SALTS | MENTHOL 15% SMELLING SALTS | Hubei Minxin Pharmaceutical Co., Ltd. | 5a78d096-4740-8dd4-e063-6294a90a651f | 2026-09-09 | Warnings | L7T10EIP3A |
| Wart Corn Remover | SALICYLIC ACID | HONG KONG FOREVER YOUNG TRADING CO., LIMITED | 5b0cd6e0-f220-4ebd-e063-6294a90ade67 | 2026-09-09 | Warnings | M017 |
| Magic Cream | PAIN RELIEVING OINTMENT | Jiangxi Baikang Medical Products Co., Ltd. | 5b0f2515-47e9-603f-e063-6294a90af9d4 | 2026-09-09 | Warnings | M017 L7T10EIP3A |
| Burn Gel | LIDOCAINE HCI | Trifecta Pharmaceuticals USA LLC | e9d3e9be-1036-fad0-e053-2a95a90a6efe | 2026-09-09 | Warnings | M017 |
| 4% Lidocaine Pain Relief Patch | LIDOCAINE 4% | Guangxi Keyun E-commerce Co., Ltd. | 5b197cd8-542f-38b4-e063-6294a90ad7d3 | 2026-09-09 | Warnings | M017 |
| Alcohol Prep Pad Medium | ALCOHOL PREP PAD | Yangzhou Huanrui Medical Technology Co., Ltd | 5af3eedc-d01e-c9e9-e063-6394a90a49e1 | 2026-09-08 | Warnings | ND2M416302 |
| Verifine | ALCOHOL SWABS | Promisemed Hangzhou Meditech Co., LTD | 5af9f31b-0c92-e3a9-e063-6394a90a38c9 | 2026-09-08 | Warnings | ND2M416302 |
| Verifine | ALCOHOL SWABS | Promisemed Hangzhou Meditech Co., LTD | 5afc0201-490e-ccf3-e063-6394a90aadad | 2026-09-08 | Warnings | ND2M416302 |
| Sting Relief Pad | BENZOCAINE, ISOPROPYL ALCOHOL CLOTH | JINHUA JINGDI MEDICAL SUPPLIES CO., LTD | 57ccc28b-5f5f-30ec-e063-6294a90a081c | 2026-09-07 | Warnings | ND2M416302 |
| Pain Relieving Lidocaine Patch | LIDOCAINE | YYBA CORP | af8c84fd-224c-72b3-e053-2a95a90a9568 | 2026-09-07 | Warnings | M017 |
| American Safety First Aid | LIDOCAINE HCL | Orazen Inc | ea2f776b-dfd0-6ce4-e053-2995a90af009 | 2026-09-07 | Warnings | M017 |
| MEDI-FIRST Topical Analgesic | LIDOCAINE HCI | Ultra Distributors Inc | b6f288f7-9ae3-215e-e053-2a95a90aedf6 | 2026-09-07 | Warnings | M017 |
| ALCOHOL PREP PADS MEDIUM STERILE | ISOPROPYL ALCOHOL CLOTH | JINHUA JINGDI MEDICAL SUPPLIES CO., LTD | 57cbbe72-24ec-2e4a-e063-6394a90abbd2 | 2026-09-07 | Warnings | ND2M416302 |
| MEDI-FIRST | BENZALKONIUM CHLORIDE, LIDOCAINE | Orazen Inc | f508434f-5948-7134-e053-2a95a90a03d7 | 2026-09-05 | Warnings | M017 |
| MEDI-FIRST | BENZALKONIUM CHLORIDE, LIDOCAINE | Orazen Inc | f522fb0b-3d86-b228-e053-2a95a90a55e9 | 2026-09-05 | Warnings | M017 |
| SurviveX PREP WIPES | ALCOHOL PREP PAD | Changzhou Maokang Medical Products Co., Ltd. | 5a7e9dc6-cf43-7ffc-e063-6394a90a3faa | 2026-09-04 | Warnings | ND2M416302 |
| SurviveX Anti-itch Cream | SURVIVEX HYDROCORTISONE | Nantong Health & Beyond Hygienic Products Inc. | 5a7a1141-d3b1-0ee8-e063-6294a90a16aa | 2026-09-04 | Warnings | M017 |
| Nerve Guard Nerve Relief | LIDOCAINE HYDROCHLORIDE, MENTHOL,MAGNESIUM CHLORIDE | Micelle Laboratories, Incorporated | 6b78f40f-2a7f-4c49-96af-1a95acbf430f | 2026-09-04 | Warnings | L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.