"44911-0536-1" National Drug Code (NDC)

NDC Code	44911-0536-1
Package Description	30 mL in 1 BOTTLE, DROPPER (44911-0536-1)
Product NDC	44911-0536
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Household Antigens
Non-Proprietary Name	Acetone, Sodium Tripolyphosphate, Propylene Glycol, Benzinum, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Butyl Acetate, Ethyl Acetate, Toluene, Xylene, Bisphenol A, Petroleum, Anacardium Orientale, Graphites, Nitricum Acidum, Pulsatilla (pratensis), Sulphur
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20200310
End Marketing Date	20280517
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Energique, Inc.
Substance Name	ACETONE; AMMONIUM CHLORIDE; ANEMONE PRATENSIS; BENZENE; BISPHENOL A; BUTYL ACETATE; ETHYL ACETATE; GRAPHITE; KEROSENE; NITRIC ACID; PROPYLENE GLYCOL; SEMECARPUS ANACARDIUM JUICE; SODIUM LAURYL SULFATE; SODIUM TRIPOLYPHOSPHATE; SULFUR; TOLUENE; TURPENTINE OIL; XYLENE (MIXED ISOMERS)
Strength	9; 9; 12; 9; 9; 9; 9; 12; 9; 12; 9; 12; 9; 9; 12; 9; 9; 9
Strength Unit	[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