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 |
|---|---|---|---|---|---|---|
| HEEL PAIN RELIEF ROLL-ON | LIDOCAINE AND MENTHOL | Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. | 4c06c4a4-557b-8bb1-e063-6294a90a9125 | 2026-03-02 | Warnings | M017 L7T10EIP3A |
| Sunburn Relief | LIDOCAINE HCL 0.5% | Old East Main Co. | 49173ec8-c94a-44c9-8a13-0f4b01b96cd6 | 2026-03-02 | Warnings, Adverse reactions | M017 |
| Antispetic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Old East Main Co. | 468c9f98-b98a-4a82-a9e0-7333c4ae372f | 2026-03-02 | Warnings, Adverse reactions | L7T10EIP3A |
| Isopropyl | ISOPROPYL ALCOHOL | Old East Main Co. | ea6f3065-780e-4afc-a361-a2cb296ae4d5 | 2026-03-02 | Warnings, Adverse reactions | ND2M416302 |
| Itch Relief | DIPHENHYDRAMINE HCL, ZINC ACETATE | Old East Main Co. | 6d87547f-bf4c-4dda-bd9d-32b576afd805 | 2026-03-02 | Warnings, Adverse reactions | M017 |
| Still Standing | MENTHOL, UNSPECIFIED FORM | Natural Essentials Inc. | 66974aaf-c82f-4fe9-bfb3-3430b80ac9f2 | 2026-03-02 | Warnings | M017 L7T10EIP3A |
| Mouth Rinse | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Old East Main Co. | 76554d61-ed96-4631-9140-135f1a2e282b | 2026-03-02 | Warnings, Adverse reactions | L7T10EIP3A |
| Antispetic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Old East Main Co. | 4ad54821-03fe-4f81-a2da-0cdab48441eb | 2026-03-02 | Warnings, Adverse reactions | L7T10EIP3A |
| Antispetic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Old East Main Co. | 1cfd85f3-ef19-46f6-8225-287a8a0a32fd | 2026-03-02 | Warnings, Adverse reactions | L7T10EIP3A |
| 70% | ISOPROPYL ALCOHOL | Old East Main Co. | 3e7a7f3e-3e99-4999-95c2-1603aca08e89 | 2026-03-02 | Warnings, Adverse reactions | ND2M416302 |
| 50% Rubbing | ISOPROPYL ALCOHOL | Old East Main Co. | 2b600254-2a70-4254-85fb-29b9adb56c9a | 2026-03-02 | Warnings, Adverse reactions | ND2M416302 |
| Therapain Plus | MENTHOL ROLL-ON | Epic Laboratories, LLC | 0249cfdf-b7c4-f27d-e063-6294a90aaa26 | 2026-03-02 | Warnings | L7T10EIP3A |
| Lightning Pain Relief | MENTHOL | Clinical Resolution Laboratory, Inc. | 80af21f5-dba8-42b0-8a65-ac5a94d83ca8 | 2026-03-02 | Warnings | M017 L7T10EIP3A |
| Isopropyl alcohol 91 percent | ISOPROPYL ALCOHOL | TARGET Corporation | c49f46c5-f9b2-4045-a31d-63cb22210233 | 2026-03-02 | Warnings | ND2M416302 |
| Isopropyl alcohol 91 percent | ISOPROPYL ALCOHOL | Sam's West, Inc | a9d6778a-e5ad-4e02-9142-4a932540eda7 | 2026-03-02 | Warnings | ND2M416302 |
| Icy Hot Lidocaine No-Mess | LIDOCAINE HYDROCHLORIDE | Chattem, Inc. | 347f9a18-8ab6-47d3-9610-5b4e9ca5d53a | 2026-03-02 | Warnings | M017 |
| Gold Bond Maximum Strength Foot Pain Relief | LIDOCAINE HYDROCHLORIDE | Gold Bond Co LLC | 8e469076-2f5a-4de8-8d13-a38c072b9af8 | 2026-03-01 | Warnings | M017 |
| HealthWise Pain Relief Lidocaine | LIDOCAINE HYDROCHLORIDE | Veridian Healthcare | 48ecbab9-13e0-d0fa-e063-6294a90a6ff2 | 2026-02-28 | Warnings | M017 |
| NUMBING CREAMS | LIDOCAINE | Yongchun Lihui Trading Co., Ltd. | 3b5e1a74-5946-4f1f-e063-6394a90a404b | 2026-02-27 | Warnings | M017 |
| Pain Relieving Gel | LIDOCAINE HYDROCHLORIDE | Chain Drug Marketing Association | b55b7253-2fd2-45cc-b94c-e92395ab0d2b | 2026-02-27 | Warnings, Adverse reactions | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.