NDC 43742-2196-01 - Skin Infections
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
- 43742-2196
- Requested NDC
- 43742-2196-01
- Package NDCs from labels
- 43742-2196-1, 43742-2196-01
- Manufacturer
- Deseret Biologials, Inc. | Apotheca Company
- Effective date
- 2024-08-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Skin Infections - Deseret Biologials, Inc. | Apotheca Company | Deseret Biologials, Inc. | Apotheca Company | 2024-08-30 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43742-2196-1 | Skin Infections | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43742-2196 | SKIN INFECTIONS (AILANTHUS GLANDULOSUS, ARSENICUM ALBUM, HERPES SIMPLEX VIRUS 1 AND 2 DNA, ECHINACEA (ANGUSTIFOLIA), HEPAR SULPHURIS CALCAREUM, HERPES SIMPLEX I AND II NOSODE, HERPES ZOSTER NOSODE, LACHESIS MUTUS, MERCURIUS SOLUBILIS, MEZEREUM, PHYTOLACCA DECANDRA) LIQUID [DESERET BIOLOGIALS, INC.] | 1 | Current NDC, 1 package rows | 20240831_f7b1cec1-ec09-4222-83f9-a59f4a84e904.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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.