NDC 48951-8140

Rhus Aconitum

Rhus Aconitum

Rhus Aconitum is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Gelsemium Sempervirens Root; Pseudognaphalium Luteoalbum Leaf; Aconitum Napellus; Atropa Belladonna; Mandragora Officinarum Root; Toxicodendron Pubescens Leaf; Penoxsulam.

Product ID48951-8140_6cf96c90-8ad8-48a4-e053-2991aa0a97d1
NDC48951-8140
Product TypeHuman Otc Drug
Proprietary NameRhus Aconitum
Generic NameRhus Aconitum
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc.
Substance NameGELSEMIUM SEMPERVIRENS ROOT; PSEUDOGNAPHALIUM LUTEOALBUM LEAF; ACONITUM NAPELLUS; ATROPA BELLADONNA; MANDRAGORA OFFICINARUM ROOT; TOXICODENDRON PUBESCENS LEAF; PENOXSULAM
Active Ingredient Strength4 [hp_X]/mL; [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 48951-8140-1

10 AMPULE in 1 BOX (48951-8140-1) > 1 mL in 1 AMPULE
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-8140-1 [48951814001]

Rhus Aconitum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

Drug Details

Active Ingredients

IngredientStrength
GELSEMIUM SEMPERVIRENS ROOT4 [hp_X]/mL

OpenFDA Data

SPL SET ID:a176c241-fc2d-4fea-82d9-81183971b4cf
Manufacturer
UNII

NDC Crossover Matching brand name "Rhus Aconitum" or generic name "Rhus Aconitum"

NDCBrand NameGeneric Name
48951-8140Rhus AconitumRhus Aconitum
48951-8142Rhus AconitumRhus Aconitum

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