NDC 48951-7012

Mandragora Arnica

Mandragora Arnica

Mandragora Arnica is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Betula Pubescens Leaf; Mandragora Officinarum Root; Sus Scrofa Meniscus; Formica Rufa; Arnica Montana; Equisetum Arvense Top.

Product ID48951-7012_55da9353-8716-3f5d-e054-00144ff88e88
NDC48951-7012
Product TypeHuman Otc Drug
Proprietary NameMandragora Arnica
Generic NameMandragora Arnica
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc.
Substance NameBETULA PUBESCENS LEAF; MANDRAGORA OFFICINARUM ROOT; SUS SCROFA MENISCUS; FORMICA RUFA; ARNICA MONTANA; EQUISETUM ARVENSE TOP
Active Ingredient Strength3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 48951-7012-1

10 AMPULE in 1 BOX (48951-7012-1) > 1 mL in 1 AMPULE
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-7012-1 [48951701201]

Mandragora Arnica LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

Drug Details

Active Ingredients

IngredientStrength
BETULA PUBESCENS LEAF3 [hp_X]/mL

OpenFDA Data

SPL SET ID:89f09a5f-2df1-42ed-b01e-d30023070fae
Manufacturer
UNII

NDC Crossover Matching brand name "Mandragora Arnica" or generic name "Mandragora Arnica"

NDCBrand NameGeneric Name
48951-7012Mandragora ArnicaMandragora Arnica
48951-7200Mandragora ArnicaMandragora Arnica

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