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 NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43857-0405-14385704050130 mL in 1 BOTTLE, DROPPER (43857-0405-1) 30 ml2016-08-032023-06-29NoNoCurrent