NDC 58066-7002

Skin Irritation and Itch Response

Agaricus Muscarius, Alumina, Anagallis Arvensis, Antimonium Tartaricum, Apis Mellifica, Arsenicum Album, Arsenicum Iodatum, Bovista, Causticum, Dolichos Pruriens, Fagapyrum Esculentum, Graphites, Kali Muriaticum, Lac Defloratum, Muriaticum Acidum, Oleander, Petroleum, Pix Liquida, Radium Bromatum, Rhus Toxicodendron, Selenium Metallicum, Sulphur, Urtica Urens

Skin Irritation and Itch Response is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Beaumont Bio Med. The primary component is Amanita Muscaria Fruiting Body; Aluminum Oxide; Anagallis Arvensis; Antimony Potassium Tartrate; Apis Mellifera; Arsenic Trioxide; Arsenic Triiodide; Lycoperdon Utriforme Fruiting Body; Causticum; Mucuna Pruriens Fruit Trichome; Fagopyrum Esculentum; Graphite; Potassium Chloride; Skim Milk; Hydrochloric Acid; Nerium Oleander Leaf; Kerosene; Pine Tar; Radium Bromide; Toxicodendron Pubescens Leaf; Selenium; Sulfur; Urtica Urens.

Product ID58066-7002_7a6df16b-e570-419a-9b7c-0d87c0c0c5a8
NDC58066-7002
Product TypeHuman Otc Drug
Proprietary NameSkin Irritation and Itch Response
Generic NameAgaricus Muscarius, Alumina, Anagallis Arvensis, Antimonium Tartaricum, Apis Mellifica, Arsenicum Album, Arsenicum Iodatum, Bovista, Causticum, Dolichos Pruriens, Fagapyrum Esculentum, Graphites, Kali Muriaticum, Lac Defloratum, Muriaticum Acidum, Oleander, Petroleum, Pix Liquida, Radium Bromatum, Rhus Toxicodendron, Selenium Metallicum, Sulphur, Urtica Urens
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2013-01-16
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameBeaumont Bio Med
Substance NameAMANITA MUSCARIA FRUITING BODY; ALUMINUM OXIDE; ANAGALLIS ARVENSIS; ANTIMONY POTASSIUM TARTRATE; APIS MELLIFERA; ARSENIC TRIOXIDE; ARSENIC TRIIODIDE; LYCOPERDON UTRIFORME FRUITING BODY; CAUSTICUM; MUCUNA PRURIENS FRUIT TRICHOME; FAGOPYRUM ESCULENTUM; GRAPHITE; POTASSIUM CHLORIDE; SKIM MILK; HYDROCHLORIC ACID; NERIUM OLEANDER LEAF; KEROSENE; PINE TAR; RADIUM BROMIDE; TOXICODENDRON PUBESCENS LEAF; SELENIUM; SULFUR; URTICA URENS
Active Ingredient Strength10 [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 58066-7002-7

59.2 mL in 1 BOTTLE, SPRAY (58066-7002-7)
Marketing Start Date2013-01-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58066-7002-7 [58066700207]

Skin Irritation and Itch Response LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-01-16
Inactivation Date2020-01-31

Drug Details


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