Candida Yeast
- Product NDC
- 50845-0266
- 11-digit product format
- 508450266
- Labeler code
- 50845
- Product ID
- 50845-0266_87f447b1-2229-491d-a61e-631d4b03a7c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Baptisia Tinctoria, Borax, Candida Albicans, Candida Parapsilosis, Cinchona Officinalis, Echinacea (Angustifolia), Nitricum Acidum, Pulsatilla (Pratensis), Pyrogenium, Sepia, Sulphuricum Acidum, Thuja Occidentalis
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Liddell Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-03-18
- Marketing end
- 2025-03-26
- Substance
- ANEMONE PRATENSIS; BAPTISIA TINCTORIA ROOT; CANDIDA ALBICANS; CANDIDA PARAPSILOSIS; CINCHONA OFFICINALIS BARK; ECHINACEA ANGUSTIFOLIA WHOLE; NITRIC ACID; RANCID BEEF; SEPIA OFFICINALIS JUICE; SODIUM BORATE; SULFURIC ACID; THUJA OCCIDENTALIS LEAFY TWIG
- Active strength
- 30 [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- 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]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50845-0266-1 | 50845026601 | 30 mL in 1 BOTTLE, SPRAY (50845-0266-1) | 30 ml | 2020-03-18 | 0000-00-00 | No | No | Current |