NDC 83027-0141-01 - Femmepap
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
- 83027-0141
- Requested NDC
- 83027-0141-01
- Package NDCs from labels
- 83027-0141-1, 83027-0141-01
- Manufacturer
- Nutritional Specialties, Inc.
- Effective date
- 2024-07-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| DRUG FACTS: | Nutritional Specialties, Inc. | 2024-07-25 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83027-0141-1 | Femmepap | 60 mL in 1 BOTTLE, SPRAY | SPRAY | 60 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 83027-0141 | FEMMEPAP (THUJA OCCIDENTALIS, NITRICUM ACIDUM, CAUSTICUM, SABINA, ANTIMONIUM SULPHURATUM RUBRUM, HUMAN PAPILLOMA NOSODE, X-RAY, ADENOVIREN NOSODE) SPRAY [NUTRITIONAL SPECIALTIES, INC.] | 1 | Current NDC, 1 package rows | 20240726_69121519-3b95-4811-87f1-3f8a0d532f69.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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.