Rub the pain Away
- Manufacturer
- Fullstack Fulfillment
- Effective date
- 2026-01-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 01:34:24
Label at a glance#
ProductPain Relief
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, CAPSAICIN
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 6c13b22c-b3ba-4127-b768-0132dd5ab0d1 | Product name | 1 | 20230829 |
| 473d070d-1c38-488e-b991-c4d1bf45aab8 | Product name | 1 | 20210201 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83084-265-04 | Pain Relief | 108 g in 1 BOTTLE, PLASTIC | SPRAY | 108 | 3 |
Products#
Every source-derived product name is available through these pages.
- Pain Relief
- Analgesic
- ISOPROPYL ALCOHOL
- CAMPHOR (SYNTHETIC)
- DIMETHICONE
- SILICON DIOXIDE
- PHENOXYETHANOL
- PALM OIL
- MENTHOL
- CAPSAICIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 83084-265 | 83084-265-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ISOPROPYL ALCOHOL | ND2M416302 | IACT |
| CAMPHOR (SYNTHETIC) | 5TJD82A1ET | ACTIB |
| DIMETHICONE | 92RU3N3Y1O | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| PALM OIL | 5QUO05548Z | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
| CAPSAICIN | S07O44R1ZM | ACTIB |
Source Document#
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 |
|---|---|---|---|---|---|---|
| Pain Relief | ANALGESIC | Fullstack Fulfillment | 2a433cee-8b6f-c280-e063-6394a90ae25a | 2026-01-21 | 83084-265-04 83084-265 83084026504 48eb9d2e-f9ba-4550-e063-6294a90a2901 2a433cee-8b6f-c280-e063-6394a90ae25a |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
