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
- 2026-10-21
- 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 | 2026-10-21 | 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 |
|---|---|---|---|---|---|---|
| LONAZEM | MENTHOL,PETROLATUM | PEER PHARM LTD. | 91f7a741-4178-4639-9cd5-746a4b9a21bf | 2026-01-12 | Warnings | L7T10EIP3A |
| Isopropyl Alcohol 50% | ISOPROPYL ALCOHOL 50% | Hydrox Laboratories | 930bb3a3-5ca3-414c-b4fb-c71ee17fc746 | 2026-01-12 | Warnings | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Hydrox Laboratories | f2f07464-6bd5-434c-8dea-0ba659c0e549 | 2026-01-12 | Warnings | ND2M416302 |
| Isopropyl Alcohol with Wintergreen 70% | ISOPROPYL ALCOHOL WITH WINTERGREEN 70% | Hydrox Laboratories | 5845f723-8866-4738-bec6-621041899f57 | 2026-01-12 | Warnings | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Hydrox Laboratories | 2042cf29-52c5-4f1e-aae6-78e025994d18 | 2026-01-12 | Warnings | ND2M416302 |
| Isopropyl Alcohol with Wintergreen 50% | ISOPROPYL ALCOHOL WITH WINTERGREEN 50% | Hydrox Laboratories | 3a15a900-2b48-487f-b252-a1a1e0d0abfc | 2026-01-12 | Warnings | ND2M416302 |
| Isopropyl Rubbing Alcohol | ISOPROPYL ALCOHOL | Discount Drug Mart | 37a6c0fb-e9c4-4a95-9539-ca5766b3a701 | 2026-01-12 | Warnings | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Discount Drug Mart | 7ac6b062-b471-4653-9d6f-de2ca8f8b014 | 2026-01-12 | Warnings | ND2M416302 |
| BLT 2 | LIDOCAINE HCL | CENTURA PHARMACEUTICALS INC | 41dc85ec-d79b-0a32-e054-00144ff8d46c | 2026-01-12 | Warnings | M017 |
| Isopropyl Rubbing Alcohol | ISOPROPYL ALCOHOL | Epic Medical Supply Corp. | 88e6418c-ceb3-4bd6-8765-b476d8bf3ff3 | 2026-01-12 | Warnings | ND2M416302 |
| Mineral Ice Pain Relieving | MENTHOL | Crown Laboratories | 7b30076a-0af6-2f74-e053-2a91aa0ae08d | 2026-01-12 | Warnings | M017 L7T10EIP3A |
| Sarna | PRAMOXINE HYDROCHLORIDE | Crown Laboratories | 19b0ce1b-e147-01a1-e063-6394a90af808 | 2026-01-12 | Warnings | M017 |
| Sarna | PRAMOXINE HYDROCHLORIDE, MENTHOL | Crown Laboratories, Inc | 19c41e75-a654-90cf-e063-6394a90a7e97 | 2026-01-12 | Warnings | M017 L7T10EIP3A |
| Itch Relief | DIPHENHYDRAMINE HCL, ZINC ACETATE | HY-VEE, INC | 48350b54-8d9a-48c4-e063-6394a90ac040 | 2026-01-12 | Warnings | M017 |
| LidoPlus Pain Relief | LIDOCAINE HYDROCHLORIDE | Centura Pharmaceuticals, Inc | 07bacc6c-60a6-4297-8663-904a22bdc040 | 2026-01-12 | Warnings | M017 |
| BlueStop Max | EXTERNAL ANALGESIC | Clavel Corporation | f1efb51c-5217-4cb2-e053-2a95a90a7f95 | 2026-01-12 | Warnings | M017 L7T10EIP3A |
| BlueStop Max | EXTERNAL ANALGESIC | Clavel Corporation | f2277e27-868b-57ef-e053-2a95a90abf28 | 2026-01-12 | Warnings | M017 |
| BLT 3 | TETRACAINE | CENTURA PHARMACEUTICALS INC | 401a0d22-1181-02ac-e054-00144ff88e88 | 2026-01-12 | Warnings | M017 |
| Sting Relief Prep Pad | BENZOCAINE | NINGBO TIANBO FIRST AID PRODUCT CO., LTD. | 0c901f64-6890-45c0-9ca7-ee9de87903c4 | 2026-01-12 | Warnings | M017 |
| Alcohol Prep Pads | ISOPROPYL ALCOHOL | NINGBO TIANBO FIRST AID PRODUCT CO., LTD. | 3cce065a-0254-43ad-a96f-aae6979997be | 2026-01-12 | Warnings | ND2M416302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.