warnings
Warnings: For external use only When using this product: Use only as directed. Avoid contact with eyes or mucous membranes. Do not apply to wounds or damaged skin. Do not bandage tightly.
Original 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
- Original Pain Relief
- Generic name
- TOPICAL ANALGESIC LOTION
- Manufacturer
- Real Time Pain Relief Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 579bd303-9a50-4d66-e063-6294a90a6141
- SPL ID
- 579bd303-9a51-4d66-e063-6294a90a6141
- Version
- 1
- Effective date
- 2026-07-27
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:07:42
| Harmonized routes |
|---|
| TOPICAL |
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 |
|---|---|---|---|
| application number | M017 | openfda.application_number | |
| brand name | Original Pain Relief | openfda.brand_name | |
| generic name | TOPICAL ANALGESIC LOTION | openfda.generic_name | |
| manufacturer name | Real Time Pain Relief Inc | openfda.manufacturer_name | |
| ndc | package | 84573-100-01 | openfda.package_ndc |
| ndc | package | 84573-100-04 | openfda.package_ndc |
| ndc | package | 84573-100-05 | openfda.package_ndc |
| ndc | package | 84573-100-06 | openfda.package_ndc |
| ndc | package | 84573-100-03 | openfda.package_ndc |
| ndc | package | 84573-100-02 | openfda.package_ndc |
| ndc | product | 84573-100 | openfda.product_ndc |
| ndc11 | package | 84573010006 | derived:openfda.package_ndc |
| ndc11 | package | 84573010002 | derived:openfda.package_ndc |
| ndc11 | package | 84573010001 | derived:openfda.package_ndc |
| ndc11 | package | 84573010005 | derived:openfda.package_ndc |
| ndc11 | package | 84573010004 | derived:openfda.package_ndc |
| ndc11 | package | 84573010003 | derived:openfda.package_ndc |
| rxcui | 240896 | openfda.rxcui | |
| spl id | 579bd303-9a51-4d66-e063-6294a90a6141 | id | |
| spl set id | 579bd303-9a50-4d66-e063-6294a90a6141 | set_id | |
| unii | L7T10EIP3A | 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.