NDC product
Fem Flora Defense
NDC 50845-0274 · Liddell Laboratories, Inc.
Key facts
| Product NDC | 50845-0274 |
|---|---|
| Proprietary name | Fem Flora Defense |
| Nonproprietary name | Baptisia Tinctoria, Borax, Candida Albicans, Candida Parapsilosis, Cinchona Officinalis, Echinacea (Angustifolia), Nitricum Acidum, Pulsatilla (Pratensis), Pyrogenium, Sepia, Sulphuricum Acidum, Thuja Occidentalis |
| Substances | BAPTISIA TINCTORIA ROOT, SODIUM BORATE, CANDIDA ALBICANS, CANDIDA PARAPSILOSIS, CINCHONA OFFICINALIS BARK, ECHINACEA ANGUSTIFOLIA WHOLE, NITRIC ACID, PULSATILLA PRATENSIS WHOLE, RANCID BEEF, SEPIA OFFICINALIS JUICE, SULFURIC ACID, THUJA OCCIDENTALIS LEAFY TWIG |
| Dosage form | SPRAY |
| Route | ORAL |
| Labeler | Liddell Laboratories, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC] |
| Marketing start | Apr 22, 2021 |
| 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: