warnings
Warnings: If symptoms worsen or persist for more than 7 days consult a physician. If pregnant or breastfeeding consult a healthcare professional before use. Keep out of reach of children.
Dr. Nenninger Cold and Sinus Solution
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
- Dr. Nenninger Cold and Sinus Solution
- Generic name
- ALLIUM CEPA, HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, KALI IODATUM, NATRUM MURIATICUM, PULSATILLA
- Manufacturer
- Nenningers Naturals, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1e26b25c-5d93-4f69-aa9e-a187abd6d035
- SPL ID
- 46cb30fe-93a8-70dc-e063-6394a90aacf5
- Version
- 9
- Effective date
- 2025-12-25
- Source export date
- 2026-09-28
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:41:02
| 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 | Dr. Nenninger Cold and Sinus Solution | openfda.brand_name | |
| generic name | ALLIUM CEPA, HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, KALI IODATUM, NATRUM MURIATICUM, PULSATILLA | openfda.generic_name | |
| manufacturer name | Nenningers Naturals, LLC | openfda.manufacturer_name | |
| ndc | package | 42731-062-01 | openfda.package_ndc |
| ndc | product | 42731-062 | openfda.product_ndc |
| ndc11 | package | 42731006201 | derived:openfda.package_ndc |
| spl id | 46cb30fe-93a8-70dc-e063-6394a90aacf5 | id | |
| spl set id | 1e26b25c-5d93-4f69-aa9e-a187abd6d035 | set_id | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | 492225Q21H | openfda.unii | |
| unii | ZW3Z11D0JV | openfda.unii | |
| unii | 1C4QK22F9J | openfda.unii | |
| unii | T4423S18FM | openfda.unii | |
| unii | I76KB35JEV | openfda.unii | |
| unii | 1MBW07J51Q | 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.