NDC product
Femmepap
NDC 83027-0141 · Nutritional Specialties, Inc.
Key facts
| Product NDC | 83027-0141 |
|---|---|
| Proprietary name | Femmepap |
| Nonproprietary name | Thuja Occidentalis, Nitricum Acidum, Causticum, Sabina, Antimonium Sulphuratum Rubrum, Human Papilloma Nosode, X-Ray, Adenoviren Nosode |
| Substances | THUJA OCCIDENTALIS LEAFY TWIG, NITRIC ACID, CAUSTICUM, JUNIPERUS SABINA LEAFY TWIG, ANTIMONY OXIDE SULFIDE, HUMAN PAPILLOMAVIRUS, ALCOHOL, X-RAY EXPOSED (1000 RAD), HUMAN ADENOVIRUS E SEROTYPE 4 STRAIN CL-68578 ANTIGEN |
| Dosage form | SPRAY |
| Route | ORAL |
| Labeler | Nutritional Specialties, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Actively Acquired Immunity [PE], Live Human Adenovirus Type 4 Vaccine [EPC], Vaccines, Adenovirus [Chemical/Ingredient], Live, Unattenuated [Chemical/Ingredient] |
| Marketing start | Jul 25, 2024 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: