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 |
|---|---|---|---|---|---|---|
| Antiseptic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | WALMART INC. (see also Equate) | 584b38ce-d1ef-4ecc-a887-7c96e7f9669f | 2026-08-20 | Warnings | L7T10EIP3A |
| Antiseptic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Walgreens | fb93c7f6-e025-4cf2-9997-acfe9a0debdd | 2026-08-19 | Warnings | L7T10EIP3A |
| Dr. Scholls Blister Pain Relief Complete Kit | LIDOCAINE | Scholl's Wellness Company LLC | 58c2b35c-e1ed-7ea8-e063-6294a90a1494 | 2026-08-19 | Warnings | M017 |
| Dr. Scholls Blister Pain Relief Complete Kit | LIDOCAINE | Scholl's Wellness Company LLC | 585e740b-e4fa-d2aa-e063-6294a90a0982 | 2026-08-19 | Warnings | M017 |
| Listerine UltraClean Gum Plus Whitening Protection Cool Mint Antigingivitis/ Antiplaque Mouthwash | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Kenvue Brands LLC | 5965eb2a-1261-5258-e063-6294a90a7c2d | 2026-08-19 | Warnings | L7T10EIP3A |
| Ludens Honey Licorice Throat Drops | MENTHOL | Prestige Brands Holdings, Inc. | 5dc2baec-a9ed-4f6b-a7ed-76a5d35739ac | 2026-08-19 | Warnings | L7T10EIP3A |
| Ludens Dual Relief | PECTIN AND MENTHOL | Prestige Brands Holdings, Inc. | d0213cb3-ec8e-40cc-82c9-694032f0490f | 2026-08-19 | Warnings | L7T10EIP3A |
| ClaraVie | MENTHOL, ZINC OXIDE | Gentell LLC | 596c467f-a056-ea78-e063-6394a90a79f2 | 2026-08-19 | Warnings | L7T10EIP3A |
| Eagle Brand Muscular Balm | MENTHOL, METHYL SALICYLATE | PT. EAGLE INDO PHARMA | 0822bcde-a8ad-be95-e063-6294a90ad208 | 2026-08-19 | Warnings | M017 L7T10EIP3A |
| ANTI ITCH | HYDROCORTISONE | HyVee Inc | 1ab6bbb8-2b91-4c53-9168-b1e85ac296e9 | 2026-08-19 | Warnings | M017 |
| hydrocortisone 1 | HYDROCORTISONE | Kroger Company | f05edff2-2dc5-427c-b52c-518e0aaef4e0 | 2026-08-19 | Warnings | M017 |
| inControl alcohol | ISOPROPYL ALCOHOL | H-E-B | 45dfbd7a-0ae1-4146-9527-5483c884e636 | 2026-08-18 | Warnings | ND2M416302 |
| MedPride | HYDROCORTISONE | Shield Line LLC | 2f15d3b3-d1e6-4742-9eac-f956c0ffbba4 | 2026-08-18 | Warnings | M017 |
| Pain Relieving Cream Analgesic | MENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATE | Garcoa, Inc. | 2f736307-5cd4-4a76-9044-4aeecba096cc | 2026-08-18 | Warnings | M017 L7T10EIP3A |
| Lidocaine Pain Relief Roll on | PAIN RELIEF ROLL ON | NeilMed Pharmaceuticals Inc | 58ff9d2d-99e6-8f98-e063-6394a90a8de7 | 2026-08-17 | Warnings | M017 |
| 70% Isopropyl Rubbing Alcohol | ISOPROPYL RUBBING ALCOHOL | The Kroger Co. | b127bba1-ce0b-4142-8b7d-f12f062b0938 | 2026-08-17 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | The Kroger Co. | cd3f8779-9e57-4b23-a029-7424d4d4ab2a | 2026-08-17 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | The Kroger Co. | ca6c7f8a-d41a-4d77-817c-3dbdc40f890e | 2026-08-17 | Warnings, Adverse reactions | ND2M416302 |
| Hydrocortisone with Aloe | HYDROCORTISONE CREAM 1/2% | Sun Pharmaceutical Industries, Inc. | 59337940-c9be-58af-e063-6394a90abe13 | 2026-08-16 | Warnings | M017 |
| SIERQ Numbing | MENTHOL | Putian Licheng District Zhijiancheng Trading Co., Ltd. | 5936c070-d8e4-56e8-e063-6294a90a5600 | 2026-08-16 | Warnings | M017 L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.