Pneumotox
- Product NDC
- 43857-0405
- 11-digit product format
- 438570405
- Labeler code
- 43857
- Product ID
- 43857-0405_02a122f8-3aaa-413a-b1dd-0383be133a49
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Triticum Aestivum, Alfalfa, Arnica Montana, Asclepias Tuberosa, Chamomilla, Echinacea (Angustifolia), Eucalyptus Globulus, Fucus Vesiculosus, Hordeum Vulgare, Laminaria Digitata, Nasturtium Aquaticum, Plantago Major, Raphanus Sativus, Trifolium Pratense, Trigonella Foenum-Graecum, Symphytum Officinale, Lung (Suis), Oryza Sativa, Silicea, Acetone, Sodium Tripolyphosphate, Propylene Glycol, Sodium Benzene Sulfonate, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Arsenicum Album
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-08-03
- Marketing end
- 2023-06-29
- Substance
- TRITICUM AESTIVUM WHOLE; ALFALFA; ARNICA MONTANA; ASCLEPIAS TUBEROSA ROOT; MATRICARIA RECUTITA; ECHINACEA ANGUSTIFOLIA; EUCALYPTUS GLOBULUS LEAF; FUCUS VESICULOSUS; HORDEUM VULGARE TOP; LAMINARIA DIGITATA; NASTURTIUM OFFICINALE; PLANTAGO MAJOR; RAPHANUS SATIVUS; TRIFOLIUM PRATENSE FLOWER; TRIGONELLA FOENUM-GRAECUM WHOLE; SYMPHYTUM OFFICINALE WHOLE; SUS SCROFA LUNG; ORYZA SATIVA WHOLE; SILICON DIOXIDE; ACETONE; SODIUM TRIPOLYPHOSPHATE; PROPYLENE GLYCOL; SODIUM BENZENESULFONATE; AMMONIUM CHLORIDE; SODIUM LAURYL SULFATE; TURPENTINE OIL; ARSENIC TRIOXIDE; SODIUM CHLORIDE; NITRIC ACID; OENANTHE AQUATICA FRUIT; PHOSPHORIC ACID; PHOSPHORUS; PULSATILLA VULGARIS; TOXICODENDRON PUBESCENS LEAF; PARAFFIN; ETHYLENE GLYCOL; PROPYL ALCOHOL; PALMITIC ACID; DIMETHICONE; POLYACRYLIC ACID (8000 MW); GLUTARAL; METHYL METHACRYLATE; ANHYDROUS CITRIC ACID; TARTARIC ACID; ANTHRAQUINONE; HYDROGEN PEROXIDE; GLYCOLIC ACID; AMMONIUM THIOGLYCOLATE; SODIUM CARBONATE; MONOETHANOLAMINE; TOLUENE-2,5-DIAMINE; P-AMINOPHENOL
- Active strength
- 1 [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_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; 1/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 |
|---|
| 43857-0405-1 | 43857040501 | 30 mL in 1 BOTTLE, DROPPER (43857-0405-1) | 30 ml | 2016-08-03 | 2023-06-29 | No | No | Current |