Pain Relief
- Product NDC
- 54973-4009
- Requested package NDC
- 54973-4009-1
- 11-digit product format
- 549734009
- Labeler code
- 54973
- Product ID
- 54973-4009_fb360897-c464-de3b-e053-6294a90a6e36
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DIBASIC POTASSIUM PHOSPHATE,HYPERICUM PERFORATUM,TOXICODENDRON PUBESCENS LEAF,BRYONIA ALBA ROOT and MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hyland's Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-04-03
- Substance
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; TOXICODENDRON PUBESCENS LEAF; DIBASIC POTASSIUM PHOSPHATE; BRYONIA ALBA ROOT; HYPERICUM PERFORATUM
- Active strength
- 12; 6; 6; 6; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- Pharmacologic classes
- Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE | 12 [hp_X]/1 |
| TOXICODENDRON PUBESCENS LEAF | 6 [hp_X]/1 |
| DIBASIC POTASSIUM PHOSPHATE | 6 [hp_X]/1 |
| BRYONIA ALBA ROOT | 6 [hp_X]/1 |
| HYPERICUM PERFORATUM | 6 [hp_X]/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| HF539G9L3Q | Internal UNII lookup |
| 6IO182RP7A | Internal UNII lookup |
| CI71S98N1Z | Internal UNII lookup |
| T7J046YI2B | Internal UNII lookup |
| XK4IUX8MNB | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| a57ac701-c42d-6b2f-e053-2995a90a112d | Available on FDA.report |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54973-4009-1 | Pain Relief | 100 in 1 BOTTLE | TABLET | 100 | 4 | |
| 54973-4009-1 | Pain Relief | 1 in 1 CARTON | TABLET | 1 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 54973-4009 | PAIN RELIEF (DIBASIC POTASSIUM PHOSPHATE,HYPERICUM PERFORATUM,TOXICODENDRON PUBESCENS LEAF,BRYONIA ALBA ROOT AND MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE) TABLET [HYLAND'S INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20230510_a57ac701-c42d-6b2f-e053-2995a90a112d.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 |
|---|---|---|---|---|---|---|
| Pain Relief | DIBASIC POTASSIUM PHOSPHATE,HYPERICUM PERFORATUM,TOXICODENDRON PUBESCENS LEAF,BRYONIA ALBA ROOT AND MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE | Hyland's Inc. | a57ac701-c42d-6b2f-e053-2995a90a112d | 2023-05-08 | Warnings | 54973-4009-1 54973-4009 54973400901 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 54973-4009-1 | 54973400901 | 1 BOTTLE in 1 CARTON (54973-4009-1) / 100 TABLET in 1 BOTTLE | 1 bottle | 2020-04-03 | 0000-00-00 | No | No | Current |