Nausia
- Product NDC
- 43742-1314
- 11-digit product format
- 437421314
- Labeler code
- 43742
- Product ID
- 43742-1314_be2f5366-0c20-4c01-8682-80038f7152f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zingiber Officinale, Ipecacuanha, Iris Versicolor, Lac Defloratum, Lacticum Acidum, Cyclamen Europaeum, Petroleum, Tabacum, Arsenicum Album, Bryonia (Alba), Cadmium Sulphuratum, Cocculus Indicus, Colchicum Autumnale, Conium Maculatum, Ferrum Metallicum, Nux Vomica, Pulsatilla (Pratensis), Sepia, Theridion, Euphorbia Corollata
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-11-08
- Marketing end
- 2024-01-21
- Substance
- ANAMIRTA COCCULUS SEED; ANEMONE PRATENSIS; ARSENIC TRIOXIDE; BRYONIA ALBA ROOT; CADMIUM SULFIDE; COLCHICUM AUTUMNALE BULB; CONIUM MACULATUM FLOWERING TOP; CYCLAMEN PURPURASCENS TUBER; EUPHORBIA COROLLATA ROOT; GINGER; IPECAC; IRIS VERSICOLOR ROOT; IRON; KEROSENE; LACTIC ACID, DL-; SEPIA OFFICINALIS JUICE; SKIM MILK; STRYCHNOS NUX-VOMICA SEED; THERIDION CURASSAVICUM; TOBACCO LEAF
- Active strength
- 12 [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
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS]
- 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 |
|---|
| 43742-1314-1 | 43742131401 | 30 mL in 1 BOTTLE, DROPPER (43742-1314-1) | 30 ml | 2018-11-08 | 2024-01-21 | No | No | Current |