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 |
|---|---|---|---|---|---|---|
| FIRSTAR BURN | LIDOCAINE HYDROCHLORIDE | Nantong Health & Beyond Hygienic Products Inc. | 186343c5-2e71-49c4-8d64-5fb3131239fa | 2026-05-04 | Warnings | M017 |
| Feminine Anti Itch Cream | BENZOCAINE,RESORCINOL | TRIFECTA PHARMACEUTICALS USA LLC | 50c3acbf-b873-908a-e063-6294a90a66b7 | 2026-05-01 | Warnings | M017 |
| Redicare Alcohol Prep Pads | MEDIUM ALCOHOL PREP PADS | Redicare LLC | 3cb7fba1-1d2d-f4da-e063-6394a90a4b21 | 2026-05-01 | Warnings | ND2M416302 |
| 24 7 Relief and Recovery Pain Relieving | MENTHOL, UNSPECIFIED FORM | Triplicare Inc | 53ca807b-3ec2-4b5e-aa5a-6dcb756bb423 | 2026-04-30 | Warnings | M017 L7T10EIP3A |
| 70% | ISOPROPYL ALCOHOL | Your Military Exchanges | 3dcb8422-827d-479b-ba18-eee8dbb762e1 | 2026-04-30 | Warnings, Adverse reactions | ND2M416302 |
| FIRST AID BURN | LIDOCAINE HYDROCHLORIDE,BENZALKONIUM CHLORIDE | 4 Visions LLC | 50b1351d-72dd-e0c9-e063-6294a90ac743 | 2026-04-30 | Warnings | M017 |
| TheraCare Flexible Pain Relieving | LIDOCAINE | Veridian Healthcare | 4f108002-2cae-0671-e063-6294a90ab6cf | 2026-04-30 | Warnings | M017 |
| Pain Relief Gel Roll On | MENTHOL | Trifecta Pharmaceuticals USA | 50b1a420-d5cd-6d61-e063-6294a90a0451 | 2026-04-30 | Warnings | M017 L7T10EIP3A |
| Dr. Numb | LIDOCAINE AND BENZETHONIUM CHLORIDE CREAM | Shinpharma Inc | d8cdccdb-775b-4970-a6ea-50b62df221d6 | 2026-04-30 | Warnings | M017 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Perrigo Direct, Inc | 11d89d11-103e-4ef6-a996-65cff67f9b32 | 2026-04-29 | Warnings, Adverse reactions | ND2M416302 |
| Isopropyl Alcohol | ISOPROPYL ALCOHOL | Walmart Inc. | 1fd3d29f-7da0-c5ba-e063-6294a90add16 | 2026-04-29 | Warnings, Adverse reactions | ND2M416302 |
| Halls Sugar Free Mountain Menthol | MENTHOL | Mondelez Global LLC | 509f233e-ff01-8927-e063-6394a90a9929 | 2026-04-29 | Warnings | L7T10EIP3A |
| hydrocortisone | HYDROCORTISONE | Padagis Israel Pharmaceuticals Ltd | 2dc7f76f-f9ad-46ba-8b41-952e1c15f052 | 2026-04-29 | Warnings | M017 |
| anti itch | HYDROCORTISONE | HyVee Inc | e1db3641-2e83-4fec-8394-98d0d876ce0d | 2026-04-29 | Warnings | M017 |
| Eagle Brand Medicated Roll On | MENTHOL, METHYL SALICYLATE | PT. EAGLE INDO PHARMA | 50805eee-33b3-86bd-e063-6294a90a77d8 | 2026-04-28 | Warnings | M017 L7T10EIP3A |
| FixMySkin Healing Balm Vanilla Flavor | HYDROCORTISONE | Lovely Skin, Inc. | 52f7a561-a0b5-4562-a588-d74fd874b83a | 2026-04-28 | Warnings | M017 |
| Blue Star Medicated | CAMPHOR | Focus Consumer Healthcare, LLC | 56df008e-a23b-4870-e054-00144ff8d46c | 2026-04-27 | Warnings | M017 5TJD82A1ET |
| Eagle Brand Muscle Rub | MENTHOL, METHYL SALICYLATE | Borden Company (Private) Limited | 06cb845c-cc53-1f1d-e063-6394a90a8c01 | 2026-04-27 | Warnings | M017 L7T10EIP3A |
| Eagle Brand Medicated Oil Aromatic | CAMPHOR, MENTHOL, METHYL SALICYLATE | PT. EAGLE INDO PHARMA | 0ef7c3aa-94a3-9fe9-e063-6394a90ab13d | 2026-04-27 | Warnings | M017 L7T10EIP3A 5TJD82A1ET |
| Eagle Brand Medicated Oil | MENTHOL, METHYL SALICYLATE | PT. EAGLE INDO PHARMA | 5071f145-49f7-0855-e063-6394a90a8f26 | 2026-04-27 | Warnings | M017 L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.