Candida Plus
- Product NDC
- 43742-1200
- 11-digit product format
- 437421200
- Labeler code
- 43742
- Product ID
- 43742-1200_f486861f-ec78-492f-90af-aedc22c4104c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea (Angustifolia), Allium Sativum, Asafoetida, Hydrastis Canadensis, Berberis Vulgaris, Borax, Saccharum Officinale, Acetaldehyde, Caffeinum, Gallicum Acidum, Indolum, Folliculinum, Lycopodium Clavatum, Phytolacca Decandra, Pulsatilla (Pratensis), Sepia, Ustilago Maidis, Torula Cerevisiae
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-04-05
- Marketing end
- 2023-05-23
- Substance
- ECHINACEA ANGUSTIFOLIA; GARLIC; FERULA ASSA-FOETIDA RESIN; GOLDENSEAL; BERBERIS VULGARIS ROOT BARK; SODIUM BORATE; SUCROSE; ACETALDEHYDE; CAFFEINE; GALLIC ACID MONOHYDRATE; INDOLE; ESTRONE; LYCOPODIUM CLAVATUM SPORE; PHYTOLACCA AMERICANA ROOT; ANEMONE PRATENSIS; SEPIA OFFICINALIS JUICE; USTILAGO MAYDIS; SACCHAROMYCES CEREVISIAE
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-1200-1 | 43742120001 | 30 mL in 1 BOTTLE, DROPPER (43742-1200-1) | 30 ml | 2018-04-05 | 2023-05-23 | No | No | Current |