NDC 37662-0322-01 - Cinnabaris
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 37662-0322
- Requested NDC
- 37662-0322-01
- Package NDCs from labels
- 37662-0322-1, 37662-0322-2, 37662-0322-3, 37662-0322-01
- Manufacturer
- Hahnemann Laboratories, INC.
- Effective date
- 2022-06-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Cinnabaris - Hahnemann Laboratories, INC. | Hahnemann Laboratories, INC. | 2022-06-03 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 37662-0322-1 | Cinnabaris | 200 in 1 VIAL, GLASS | PELLET | 200 | 1 | |
| 37662-0322-2 | Cinnabaris | 1200 in 1 BOTTLE, GLASS | PELLET | 1200 | 1 | |
| 37662-0322-3 | Cinnabaris | 4000 in 1 BOTTLE, GLASS | PELLET | 4000 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 37662-0322 | CINNABARIS PELLET [HAHNEMANN LABORATORIES, INC.] | 1 | Current NDC, Legacy NDC, 3 package rows | 20220604_e093713d-a0f5-cc29-e053-2995a90aa2e3.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Nasal Decongestant | CAMELLIA SINENSIS, EPHEDRA VULGARIS, BELLADONNA, ARSENICUM ALBUM, CINNABARIS, KALI BICHROMICUM, PULSATILLA, SEPIA, CALCAREA CARBONICA, MERCURIUS SOLUBILIS, SULPHUR | Natural Creations, Inc | 938a25f8-e854-4537-a04d-5e2276199f5c | 2018-12-21 | Warnings | ZI0T668SF1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.