Homeopathic Pain Relief Balm Active Ingredients and Purpose Section
- Manufacturer
- Neutripure Corporation
- Effective date
- 2026-04-28
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:38:26
Label at a glance#
ProductHomeopathic Pain Relief Balm
Active ingredientCOMMIPHORA MYRRHA WHOLE, BOSWELLIA SERRATA WHOLE
Label structure8 sections
Label contents#
Full prescribing information#
Homeopathic Pain Relief Balm Keep Out of Reach of Children Section
Homeopathic Pain Relief Balm Dosage and Administration (Directions) Section
Homeopathic Pain Relief Balm Inactive ingredient Section
Homeopathic Pain Relief Balm Indications and Usage Section
Homeopathic Pain Relief Balm Warnings Section
Homeopathic Pain Relief Balm Purpose Section
Homepathic Pain Relief Balm PDP
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84808-001-01 | Homeopathic Pain Relief Balm | 1 in 1 CONTAINER | OIL | 1 | 2 |
Products#
Every source-derived product name is available through these pages.
- Homeopathic Pain Relief Balm
- COMMIPHORA MYRRHA WHOLE
- COCONUT OIL
- BOSWELLIA SERRATA WHOLE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 84808-001 | 84808-001-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| COMMIPHORA MYRRHA WHOLE | UU81N77RI7 | ACTIB |
| COCONUT OIL | Q9L0O73W7L | IACT |
| BOSWELLIA SERRATA WHOLE | X7B7P649WQ | 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 |
|---|---|---|---|---|---|---|
| Homeopathic Pain Relief Balm | HOMEOPATHIC PAIN RELIEF BALM | Neutripure Corporation | 239809af-8f5c-bbab-e063-6394a90adf4a | 2026-04-28 | Warnings | 84808-001-01 84808-001 84808000101 508891cb-fedd-89e1-e063-6294a90ae32c 239809af-8f5c-bbab-e063-6394a90adf4a |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.






