Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Fem Flora Defense NDC 50845-0274
Baptisia tinctoria root 3 [hp_X]/mL + 11 more ingredients · Spray · Oral · Liddell Laboratories, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50845-0274-1 | 50845027401 | 30 mL in 1 BOTTLE, SPRAY (50845-0274-1)Marketed from Apr 22, 2021 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Fem Flora Defense
- Generic name (nonproprietary)
- baptisia tinctoria, borax, candida albicans, candida parapsilosis, cinchona officinalis, echinacea (angustifolia), nitricum acidum, pulsatilla (pratensis), pyrogenium, sepia, sulphuricum acidum, thuja occidentalis
- Active ingredients
- Baptisia tinctoria root — 3 [hp_X]/mLSodium borate — 30 [hp_C]/mLCandida albicans — 12 [hp_X]/mLCandida parapsilosis — 8 [hp_C]/mLCinchona officinalis bark — 30 [hp_C]/mLEchinacea angustifolia whole — 3 [hp_X]/mLNitric acid — 30 [hp_C]/mLPulsatilla pratensis whole — 30 [hp_C]/mLRancid beef — 200 [hp_C]/mLSepia officinalis juice — 30 [hp_C]/mLSulfuric acid — 30 [hp_C]/mLThuja occidentalis leafy twig — 30 [hp_C]/mL
- Dosage form
- Spray
- Route
- Oral
- Labeler
- Liddell Laboratories, Inc.
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
- Identifiers
- Product ID 50845-0274_6a28ccf7-80a2-4db1-a1aa-ec417335b8aeSPL ID 6a28ccf7-80a2-4db1-a1aa-ec417335b8aeSPL set ID 8015e1cb-9ebd-4b3e-af57-92f2754fb790UNII 5EF0HWI5WU, 91MBZ8H3QO, 4D7G21HDBC, 0KZ676D44N, S003A158SB, VB06AV5US8, 411VRN1TV4, 8E272251DI, 29SUH5R3HU, QDL83WN8C2, O40UQP6WCF, 1NT28V9397UPC 0363113117967
- Pharmacologic class
- Non-Standardized Fungal Allergenic Extract
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N450845027401followed by a unit qualifier and the quantityPackage 50845-0274-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS: May temporarily relieve symptoms of Candida infections: vaginal discharge, vaginal discomfort, abdominal distention, bloating.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Excerpt only. Read the full label for complete information.