NDC 83016-331-01 - PAIN RELIEF Gel-Roll On
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
- 83016-331
- Requested NDC
- 83016-331-01
- Package NDCs from labels
- 83016-331-01, 83016-331-11, 83016-331-21
- Manufacturer
- R & Y Group, LLC | Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
- Effective date
- 2023-11-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PAIN RELIEF Gel-Roll On | R & Y Group, LLC | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 2023-11-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83016-331-01 | PAIN RELIEF Gel-Roll On | 74 mL in 1 BOTTLE | GEL | 74 | 2 | |
| 83016-331-11 | PAIN RELIEF Gel-Roll On | 1 in 1 BAG | GEL | 1 | 2 | |
| 83016-331-21 | PAIN RELIEF Gel-Roll On | 3 in 1 BAG | GEL | 3 | 2 |
DailyMed Dashboard NDC Coverage#
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.
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| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET PAIN RELIEF | 5980c527-6bcb-a846-e063-6294a90a0788 | 2026-08-20 | Warnings | L7T10EIP3A |
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| Antiseptic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | WALMART INC. (see also Equate) | 584b38ce-d1ef-4ecc-a887-7c96e7f9669f | 2026-08-20 | Warnings | L7T10EIP3A |
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| MENTOL CHINO FORTE | METHYL SALICYLATE, MENTHOL, CAMPHOR | LABORATORIOS H.G. C.A. | 12652c98-e2a8-21fc-e063-6394a90a94cb | 2026-08-17 | Warnings | L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.