warnings
Warnings Stop use and ask a doctor if ■ pain gets worse or lasts more than 7 days. ■ new symptoms occur. ■ redness or swelling is present. If pregnant or breastfeeding Ask a health professional before use. Keep out of reach of children.
Pain Relief
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Pain Relief
- Generic name
- DIBASIC POTASSIUM PHOSPHATE,HYPERICUM PERFORATUM,TOXICODENDRON PUBESCENS LEAF,BRYONIA ALBA ROOT AND MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
- Manufacturer
- Hyland's Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a57ac701-c42d-6b2f-e053-2995a90a112d
- SPL ID
- fb360897-c464-de3b-e053-6294a90a6e36
- Version
- 4
- Effective date
- 2023-05-08
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:19:33
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Pain Relief | openfda.brand_name | |
| generic name | DIBASIC POTASSIUM PHOSPHATE,HYPERICUM PERFORATUM,TOXICODENDRON PUBESCENS LEAF,BRYONIA ALBA ROOT AND MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE | openfda.generic_name | |
| manufacturer name | Hyland's Inc. | openfda.manufacturer_name | |
| ndc | package | 54973-4009-1 | openfda.package_ndc |
| ndc | product | 54973-4009 | openfda.product_ndc |
| ndc11 | package | 54973400901 | derived:openfda.package_ndc |
| spl id | fb360897-c464-de3b-e053-6294a90a6e36 | id | |
| spl set id | a57ac701-c42d-6b2f-e053-2995a90a112d | set_id | |
| unii | CI71S98N1Z | openfda.unii | |
| unii | XK4IUX8MNB | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | T7J046YI2B | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.