NDC 66579-0013

Detox and Drainage, Blood and Kidney

Arsenicum Album, Baptisia Tinctoria, Carbo Vegetabilis, Chininum Sulphuricum, Cinchona Officinalis, Conium Maculatum, Echinacea Purpurea, Ferrum Metallicum, Hydrastis Canadensis, Kali Chloricum, Mercurius Corrosivus, Serum Anguillae

Detox and Drainage, Blood and Kidney is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by New Sun Inc.. The primary component is Arsenic Trioxide; Baptisia Tinctoria Root; Activated Charcoal; Quinine Sulfate; Cinchona Officinalis Bark; Conium Maculatum Flowering Top; Echinacea Purpurea; Iron; Goldenseal; Potassium Chlorate; Mercuric Chloride; Anguilla Rostrata Blood Serum.

Product ID66579-0013_9a881380-886b-445a-941f-5938729aac41
NDC66579-0013
Product TypeHuman Otc Drug
Proprietary NameDetox and Drainage, Blood and Kidney
Generic NameArsenicum Album, Baptisia Tinctoria, Carbo Vegetabilis, Chininum Sulphuricum, Cinchona Officinalis, Conium Maculatum, Echinacea Purpurea, Ferrum Metallicum, Hydrastis Canadensis, Kali Chloricum, Mercurius Corrosivus, Serum Anguillae
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2014-09-05
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNew Sun Inc.
Substance NameARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; ACTIVATED CHARCOAL; QUININE SULFATE; CINCHONA OFFICINALIS BARK; CONIUM MACULATUM FLOWERING TOP; ECHINACEA PURPUREA; IRON; GOLDENSEAL; POTASSIUM CHLORATE; MERCURIC CHLORIDE; ANGUILLA ROSTRATA BLOOD SERUM
Active Ingredient Strength10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 66579-0013-2

59 mL in 1 BOTTLE, SPRAY (66579-0013-2)
Marketing Start Date2014-09-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 66579-0013-2 [66579001302]

Detox and Drainage, Blood and Kidney LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-09-05
Inactivation Date2020-01-31

Drug Details


© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.