warnings
WARNINGS
Mucus 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
- Mucus Relief
- Generic name
- ANTIMONY POTASSIUM TARTRATE, ATROPA BELLADONNA, BRYONIA ALBA WHOLE, ANEMONE AMERICANA, HYOSCYAMUS NIGER, IPECAC, LOBELIA INFLATA, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, AND LOBARIA PULMONARIA
- Manufacturer
- MediNatura Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 6338dc4f-b2d9-4b9a-a397-0440cbd1345a
- SPL ID
- 906bf8a5-cca6-4a15-9de3-4f4111da1c2f
- Version
- 7
- Effective date
- 2022-12-14
- Source export date
- 2026-10-12
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:56:18
| 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 | Mucus Relief | openfda.brand_name | |
| generic name | ANTIMONY POTASSIUM TARTRATE, ATROPA BELLADONNA, BRYONIA ALBA WHOLE, ANEMONE AMERICANA, HYOSCYAMUS NIGER, IPECAC, LOBELIA INFLATA, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, AND LOBARIA PULMONARIA | openfda.generic_name | |
| manufacturer name | MediNatura Inc | openfda.manufacturer_name | |
| ndc | package | 62795-1012-2 | openfda.package_ndc |
| ndc | package | 62795-1012-3 | openfda.package_ndc |
| ndc | product | 62795-1012 | openfda.product_ndc |
| ndc11 | package | 62795101203 | derived:openfda.package_ndc |
| ndc11 | package | 62795101202 | derived:openfda.package_ndc |
| spl id | 906bf8a5-cca6-4a15-9de3-4f4111da1c2f | id | |
| spl set id | 6338dc4f-b2d9-4b9a-a397-0440cbd1345a | set_id | |
| unii | 9PP1T3TC5U | openfda.unii | |
| unii | U364V64HUN | openfda.unii | |
| unii | DL6OZ476V3 | openfda.unii | |
| unii | 6ICN6T7FEM | openfda.unii | |
| unii | 4WRK2153H3 | openfda.unii | |
| unii | WQZ3G9PF0H | openfda.unii | |
| unii | 62I3C8233L | openfda.unii | |
| unii | 56K0VVT47P | openfda.unii | |
| unii | D1YM0P5Z2T | 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.