Candida Yeast
- Product NDC
- 50845-0200
- 11-digit product format
- 508450200
- Labeler code
- 50845
- Product ID
- 50845-0200_3b19a61f-8413-4446-b8ac-bd79c923c803
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Baptisia Tinctoria, Borax, Candida Albicans, Candida Parapsilosis, Echinacea (Angustifolia), Kreosotum, Mercurius Cyanatus, Mercurius Sulphuratus Ruber, Nitricum Acidum, Pyrogenium, Sulphuricum Acidum, Thuja Occidentalis
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Liddell Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-02-21
- Marketing end
- 2023-01-29
- Substance
- BAPTISIA TINCTORIA; CANDIDA ALBICANS; CANDIDA PARAPSILOSIS; ECHINACEA ANGUSTIFOLIA; MERCURIC CYANIDE; MERCURIC SULFIDE; NITRIC ACID; RANCID BEEF; SODIUM BORATE; SULFURIC ACID; THUJA OCCIDENTALIS LEAF; WOOD CREOSOTE
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_C]/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
- 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 |
|---|
| 50845-0200-1 | 50845020001 | 30 mL in 1 BOTTLE, SPRAY (50845-0200-1) | 30 ml | 2014-02-21 | 2023-01-29 | No | No | Current |