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 |
|---|---|---|---|---|---|---|
| OVERNIGHT RELIEF Gel-Patch | MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 2c6c4737-dff3-6382-e063-6294a90a412c | 2026-05-14 | Warnings | L7T10EIP3A |
| Pain Relief | MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 3ed34e65-9d74-daff-e063-6394a90a94c7 | 2026-05-14 | Warnings | L7T10EIP3A |
| MENTHOL PAIN RELIEF Gel-Patch | MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 0e6a09cc-7986-f851-e063-6294a90aff67 | 2026-05-14 | Warnings | L7T10EIP3A |
| PAIN RELIEF Gel-Patch | LIDOCAINE AND MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 3c166165-2ad8-206f-e063-6294a90a52fc | 2026-05-14 | Warnings | L7T10EIP3A |
| OVERNIGHT RELIEF Gel-Patch | MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | f1041b25-eb09-e43d-e053-2995a90a073a | 2026-05-14 | Warnings | L7T10EIP3A |
| PAIN RELIEF Gel-Patch | LIDOCAINE AND MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | f1047707-3fe5-06bc-e053-2995a90a59b9 | 2026-05-14 | Warnings | L7T10EIP3A |
| Elastic Relief Strip | MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | f103cf8a-a285-28d1-e053-2995a90ae70e | 2026-05-14 | Warnings | L7T10EIP3A |
| Halls Honey Lemon | MENTHOL | Mondelez Global LLC | aec46410-ffb1-4db4-b232-82110c562f69 | 2026-05-13 | Warnings | L7T10EIP3A |
| Pain Relief Gel-Roll On | MENTHOL | Trifecta Pharmaceuticals USA | 51b403dc-fc9b-0cad-e063-6394a90af081 | 2026-05-13 | Warnings | M017 L7T10EIP3A |
| Biofreeze | MENTHOL | Reckitt Benckiser LLC | 5edddb99-6596-4a3b-b361-1cc04d032c31 | 2026-05-13 | Warnings | M017 L7T10EIP3A |
| Biofreeze | MENTHOL | Reckitt Benckiser LLC | 684faf63-5e44-4471-8384-e8fa7c0d842a | 2026-05-13 | Warnings | M017 L7T10EIP3A |
| Biofreeze | MENTHOL | Reckitt Benckiser LLC | 4c798b06-6ee5-41d1-8a14-f6889512ade3 | 2026-05-13 | Warnings | M017 L7T10EIP3A |
| BIOFREEZE | MENTHOL | Reckitt Benckiser LLC | 83d5c2f2-2413-4d28-83b2-0808d0917b4d | 2026-05-13 | Warnings | M017 L7T10EIP3A |
| Scalpicin Anti-Itch Maximum Strength | HYDROCORTISONE | Reckitt Benckiser LLC | 7b1a29fa-b266-43e6-a87b-aa3c96ab4041 | 2026-05-13 | Warnings | M017 |
| Biofreeze Menthol | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | 3f2b1f48-2d78-4985-a046-9f72de5e1a9b | 2026-05-13 | Warnings | M017 |
| Biofreeze | MENTHOL | Reckitt Benckiser LLC | 10a8face-47da-ebbe-e063-6294a90a42fe | 2026-05-13 | Warnings | M017 L7T10EIP3A |
| Biofreeze Foot Cream | MENTHOL | Reckitt Benckiser LLC | 32450cbf-4ed4-402b-a30e-e08a17bba3fb | 2026-05-13 | Warnings | M017 L7T10EIP3A |
| Biofreeze | MENTHOL | Reckitt Benckiser LLC | a227213b-e89f-7144-e053-2a95a90a7e74 | 2026-05-13 | Warnings | M017 L7T10EIP3A |
| Biofreeze | MENTHOL | Reckitt Benckiser LLC | 00bb462a-27d0-6f74-e063-6394a90a90ec | 2026-05-13 | Warnings | M017 L7T10EIP3A |
| BioFreeze Dry Stick | MENTHOL | Reckitt Benckiser LLC | 26d62cd2-9209-8cca-e063-6394a90a2028 | 2026-05-13 | Warnings | M017 L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.