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 |
|---|---|---|---|---|---|---|
| Medi First Extra Strength Itch Relief | DIPHENHYDRAMINE, ZINC ACETATE | Unifirst First Aid Corporation | 54614e5b-8c72-d308-e063-6294a90a405d | 2026-06-16 | Warnings | M017 |
| Blue Ice Analgesic | MENTHOL | Delon Laboratories (1990) Ltd | 184ed488-6e62-40c6-bb71-1d523280fd6b | 2026-06-16 | Warnings | M017 L7T10EIP3A |
| Medi-First Hydrocortisone 1 % Anti-Itch Cream | HYDROCORTISONE | Unifirst First Aid Corporation | 49f04e5d-746d-cbe9-e063-6294a90a7e88 | 2026-06-16 | Warnings | M017 |
| Lidozall Pro | LIDOCAINE HYDROCHLORIDE | V2 Pharma LLC | ecc26ba7-4ff6-43e6-bfb9-91a9cbb509ff | 2026-06-16 | Warnings | M017 |
| 70% | ISOPROPYL ALCOHOL | Meijer, Inc. | 7b1f93ff-5eeb-4da1-8f02-7c47d713689a | 2026-06-15 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Meijer, Inc. | 531cea18-9609-4d78-876d-3ba5d2d1e16f | 2026-06-15 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Meijer, Inc. | b0d302c2-58a0-4c3e-9c4a-fd34de40c034 | 2026-06-15 | Warnings, Adverse reactions | ND2M416302 |
| Tiger Balm Pain Relieving Cool | CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM | Haw Par Healthcare Ltd. | 41590ba1-32bb-4352-97ba-d6a3cc9d0546 | 2026-06-15 | Warnings | M017 L7T10EIP3A 5TJD82A1ET |
| HIGH POTENCY PAIN RELIEF | CAPSAICIN | Xiamen Weisiqi Technology Co., Ltd. | 543949a4-86ed-3734-e063-6394a90a24f2 | 2026-06-14 | Warnings | M017 |
| Natucure HEMORRHOID | LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID | Jiangxi Yudexi Pharmaceutical Co., LTD | 49e402ed-d314-e896-e063-6294a90a826b | 2026-06-14 | Warnings | M017 |
| Nieapf NUMBING | LIDOCAINE 4% NUMBING | Jiangxi Yudexi Pharmaceutical Co., LTD | 49e7534f-bccf-4ef4-e063-6294a90aeb7f | 2026-06-14 | Warnings | M017 |
| HEALMUSZ NUMBING | HEALMUSZ NUMBING | Jiangxi Yudexi Pharmaceutical Co., LTD | 49976ff7-49a4-e4ed-e063-6294a90a3f78 | 2026-06-14 | Warnings | M017 |
| HEALMUSZ HEMORRHOID FISSURE | LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID FISSURE | Jiangxi Yudexi Pharmaceutical Co., LTD | 4a342ac0-6a8d-3408-e063-6394a90a9a10 | 2026-06-14 | Warnings | M017 |
| BOTASUN QUIT SMOKING Nicotine | NICOTINE18% MENTHOL 0.3% QUIT SMOKING NICOTINE | Jiangxi Yudexi Pharmaceutical Co., LTD | 4fa00db9-def5-dcfa-e063-6394a90ac8c2 | 2026-06-14 | Warnings | M017 L7T10EIP3A |
| HEALMUSZ NUMBING | MENTHOL 5% NUMBING | Jiangxi Yudexi Pharmaceutical Co., LTD | 4cbb7df5-5771-ce4b-e063-6294a90aab80 | 2026-06-14 | Warnings | M017 L7T10EIP3A |
| HEALMUSZ ECZEMA | HYDROCORTISONE 1% ECZEMA | Jiangxi Yudexi Pharmaceutical Co., LTD | 511e54e0-2abe-fb76-e063-6294a90ada68 | 2026-06-14 | Warnings | M017 |
| Hydrocortisone 1% Anti-ItchCream | HYDROCORTISONE | Acme United Corporation | 5425fc2b-4f25-3e64-e063-6394a90aff49 | 2026-06-13 | Warnings | M017 |
| Icy Hot Pain Relieving Balm | MENTHOL AND METHYL SALICYLATE | Chattem, Inc. | 40c8c02f-fa5f-4e80-81a0-48271fa6f94b | 2026-06-12 | Warnings | M017 L7T10EIP3A |
| Lidocaine and Menthol | LIDOCAINE AND MENTHOL | Advanced Rx of Tennessee, LLC | 44840250-2112-6ef4-e063-6394a90acdcc | 2026-06-12 | Warnings | M017 L7T10EIP3A |
| DRAWYUM Pain Relief Gel-Patch | LIDOCAINE 4% PAIN RELIEF GEL-PATCH | Jiangxi Yudexi Pharmaceutical Co., LTD | 497e6e18-ba46-0001-e063-6294a90af026 | 2026-06-12 | Warnings | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.