NDC 62106-9916

MEDULLOSSEINUM PLEX

Arnica Montana, Calcarea Phosphorica, Calendula Officinalis, Hypericum Perforatum, Medullosseinum, Pulsatilla, Ruta Graveolens, Symphytum Officinale

MEDULLOSSEINUM PLEX is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Seroyal Usa. The primary component is Hypericum Perforatum; Arnica Montana Root; Calcium Phosphate, Dibasic, Anhydrous; Comfrey Root; Pulsatilla Vulgaris; Ruta Graveolens Flowering Top; Calendula Officinalis Flowering Top; Oryctolagus Cuniculus Spinal Cord.

Product ID62106-9916_22b7eafe-ef77-0677-e054-00144ff88e88
NDC62106-9916
Product TypeHuman Otc Drug
Proprietary NameMEDULLOSSEINUM PLEX
Generic NameArnica Montana, Calcarea Phosphorica, Calendula Officinalis, Hypericum Perforatum, Medullosseinum, Pulsatilla, Ruta Graveolens, Symphytum Officinale
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2015-10-22
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameSeroyal USA
Substance NameHYPERICUM PERFORATUM; ARNICA MONTANA ROOT; CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS; COMFREY ROOT; PULSATILLA VULGARIS; RUTA GRAVEOLENS FLOWERING TOP; CALENDULA OFFICINALIS FLOWERING TOP; ORYCTOLAGUS CUNICULUS SPINAL CORD
Active Ingredient Strength5 [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 62106-9916-0

1 BOTTLE, GLASS in 1 CARTON (62106-9916-0) > 30 mL in 1 BOTTLE, GLASS
Marketing Start Date2015-10-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62106-9916-0 [62106991600]

MEDULLOSSEINUM PLEX LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-10-22

Drug Details

Active Ingredients

IngredientStrength
HYPERICUM PERFORATUM5 [hp_C]/30mL

OpenFDA Data

SPL SET ID:22b7eafe-ef76-0677-e054-00144ff88e88
Manufacturer
UNII
UPC Code
  • 0883196326808
    • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.