Solstice Pain Relieving
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
- Solstice Pain Relieving
- Generic name
- CAMPHOR, MENTHOL, METHYL SALICYLATE
- Manufacturer
- MADISON ONE ACME INC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5ef90782-8201-47d1-b57f-f032d4c9b06a
- SPL ID
- 43460d86-e2ec-0e78-e063-6294a90ae47d
- Version
- 5
- Effective date
- 2025-11-10
- 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 05:18:44
| 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 | Solstice Pain Relieving | openfda.brand_name | |
| generic name | CAMPHOR, MENTHOL, METHYL SALICYLATE | openfda.generic_name | |
| manufacturer name | MADISON ONE ACME INC | openfda.manufacturer_name | |
| ndc | package | 55614-210-02 | openfda.package_ndc |
| ndc | package | 55614-210-20 | openfda.package_ndc |
| ndc | package | 55614-210-60 | openfda.package_ndc |
| ndc | product | 55614-210 | openfda.product_ndc |
| ndc11 | package | 55614021060 | derived:openfda.package_ndc |
| ndc11 | package | 55614021002 | derived:openfda.package_ndc |
| ndc11 | package | 55614021020 | derived:openfda.package_ndc |
| rxcui | 1793147 | openfda.rxcui | |
| spl id | 43460d86-e2ec-0e78-e063-6294a90ae47d | id | |
| spl set id | 5ef90782-8201-47d1-b57f-f032d4c9b06a | set_id | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | 5TJD82A1ET | openfda.unii | |
| unii | LAV5U5022Y | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings For external use only
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Report any unexpected side effects from the use of this product to the FDA MedWatch Program
Reported adverse events (FAERS/openFDA)#
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