NDC 66343-016

Emvita 4

Platinum, Kerosene, Datura Stramonium, Apis Mellifera, Sus Scrofa Ovary, And Bos Taurus Testicle

Emvita 4 is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Rubimed Ag. The primary component is Platinum; Kerosene; Datura Stramonium; Apis Mellifera; Sus Scrofa Ovary; Bos Taurus Testicle.

Product ID66343-016_eee66b8c-2939-468c-83e0-cdcca0bcf30d
NDC66343-016
Product TypeHuman Otc Drug
Proprietary NameEmvita 4
Generic NamePlatinum, Kerosene, Datura Stramonium, Apis Mellifera, Sus Scrofa Ovary, And Bos Taurus Testicle
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2015-05-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRUBIMED AG
Substance NamePLATINUM; KEROSENE; DATURA STRAMONIUM; APIS MELLIFERA; SUS SCROFA OVARY; BOS TAURUS TESTICLE
Active Ingredient Strength800 [hp_C]/mL; [hp_M]/mL; [hp_M]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 66343-016-50

50 mL in 1 BOTTLE, DROPPER (66343-016-50)
Marketing Start Date2015-05-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 66343-016-50 [66343001650]

Emvita 4 LIQUID
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-05-07
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PLATINUM800 [hp_C]/mL

OpenFDA Data

SPL SET ID:65f430d7-a0f9-44ae-b07e-d34b27950e27
Manufacturer
UNII

NDC Crossover Matching brand name "Emvita 4" or generic name "Platinum, Kerosene, Datura Stramonium, Apis Mellifera, Sus Scrofa Ovary, And Bos Taurus Testicle"

NDCBrand NameGeneric Name
66343-016Emvita 4Platinum, Kerosene, Datura Stramonium, Apis Mellifera, Sus Scrofa Ovary, and Bos Taurus Testicle
66343-053Emvita 4Apis Mellifica, Oophorinum, Platinum met, Orchitinum, Petroleum, Stramonium
66343-091Emvita 4Apis mellifica, Orchitinum, Oophorinum, Petroleum, Platinum met, Stramonium

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