Detox
- Product NDC
- 43742-0869
- 11-digit product format
- 437420869
- Labeler code
- 43742
- Product ID
- 43742-0869_b7cda261-a149-4bcb-b223-ae56d07cb466
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Conium Maculatum, Dulcamara, Echinacea (Angustifolia), Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbic Acid, Coccus Cacti, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Pulsatilla (Vulgaris), Sarcolacticum Acidum, Lymph Node (Suis), Sulphur, Glandula Suprarenalis Suis, L-Phenylalanine, Calcarea Phosphorica, Ferrum Phosphoricum, Hepar Suis, Hypothalamus (Suis), Spleen (Suis), Cortisone Aceticum, Mercurius Solubilis, Baryta Carbonica, Glyphosate, Funiculus Umbilicalis Suis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-10-06
- Marketing end
- 2023-08-28
- Substance
- CONIUM MACULATUM FLOWERING TOP; SOLANUM DULCAMARA TOP; ECHINACEA ANGUSTIFOLIA; HORSE CHESTNUT; ANTIMONY POTASSIUM TARTRATE; ASCORBIC ACID; PROTORTONIA CACTI; GALIUM APARINE; GENTIANA LUTEA ROOT; GERANIUM ROBERTIANUM; PULSATILLA VULGARIS; LACTIC ACID, L-; SUS SCROFA LYMPH; SULFUR; SUS SCROFA ADRENAL GLAND; PHENYLALANINE; TRIBASIC CALCIUM PHOSPHATE; FERRUM PHOSPHORICUM; PORK LIVER; SUS SCROFA HYPOTHALAMUS; SUS SCROFA SPLEEN; CORTISONE ACETATE; MERCURIUS SOLUBILIS; BARIUM CARBONATE; GLYPHOSATE; SUS SCROFA UMBILICAL CORD; SUS SCROFA TONSIL; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; LIOTHYRONINE; SUS SCROFA BONE MARROW; BISPHENOL A; BROMINE; CHLORINE; HYDROFLUORIC ACID; IODINE; ESCHERICHIA COLI
- Active strength
- 4 [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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/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 |
|---|
| 43742-0869-1 | 43742086901 | 30 mL in 1 BOTTLE, DROPPER (43742-0869-1) | 30 ml | 2016-10-06 | 2023-08-28 | No | No | Current |