NDC 58214-099 - beyond nicotine kit
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
- 58214-099
- Package NDCs from labels
- 58214-099-06
- Manufacturer
- JMSP USA LLC | W Last CC
- Effective date
- 2018-11-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| beyond nicotine kit - JMSP USA LLC | W Last CC | JMSP USA LLC | W Last CC | 2018-11-10 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 58214-099-06 | beyond nicotine kit | 60 in 1 POUCH | TABLET, CHEWABLE | 1 | 6 [hp_X] in 60 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 58214-099 | BEYOND NICOTINE KIT (CALADIUM SEGUINUM, KALI SULPH, PLANTAGO MAJOR, NICOTIANA TABACUM, CALCIUM SULFATE ANHYDROUS, LOBELIA INFLATA, SAMBUCUS NIGRA FLOWERING TOP, DELPHINIUM STAPHISAGRIA SEED) KIT [JMSP USA LLC] | 2 | Unmatched | 20181128_cb60abca-aa8c-47fe-8d28-2ad836b40449.zip |
DailyMed Socrata Ingredients#
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.