43689-0031 NDC - LEG AND BACK PAIN RELIEF (ATROPA BELLADONNA,CAPSICUM,CITRULLUS COLOCYNTHIS FRUIT PULP,MAGNESIUM PHOSPHATE, DIBASIC,TOXICODENDRON RADICANS LEAF,HYPERICUM PERFORATUM)

Drug Information

Product NDC: 43689-0031

Proprietary Name: Leg and Back Pain Relief

Non Proprietary Name: ATROPA BELLADONNA,CAPSICUM,CITRULLUS COLOCYNTHIS FRUIT PULP,MAGNESIUM PHOSPHATE, DIBASIC,TOXICODENDRON RADICANS LEAF,HYPERICUM PERFORATUM

Active Ingredient(s):
  • 3 [hp_X]/113g ATROPA BELLADONNA;
  • 3 [hp_X]/113g CAPSICUM;
  • 3 [hp_X]/113g CITRULLUS COLOCYNTHIS FRUIT PULP;
  • 3 [hp_X]/113g HYPERICUM PERFORATUM;
  • 3 [hp_X]/113g MAGNESIUM PHOSPHATE, DIBASIC;
  • 3 [hp_X]/113g TOXICODENDRON RADICANS LEAF


Administration Route(s): TOPICAL

Dosage Form(s): CREAM

Pharmacy Class(es):
  • Allergens [CS];
  • Calculi Dissolution Agent [EPC];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased Large Intestinal Motility [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE];
  • Magnesium Ion Exchange Activity [MoA];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Plant Proteins [CS];
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE];
  • Vegetable Proteins [CS]

Labeler Information

Labeler Name: The Magni Group Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/8/2017

Package Information

No. Package Code Package Description Billing Unit
143689-0031-1113 g in 1 JAR (43689-0031-1)
243689-0031-21 JAR in 1 BOX (43689-0031-2) / 113 g in 1 JAR

NDC Record

Field Name Field Value Definition
PRODUCT NDC43689-0031The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMELeg and Back Pain ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEATROPA BELLADONNA,CAPSICUM,CITRULLUS COLOCYNTHIS FRUIT PULP,MAGNESIUM PHOSPHATE, DIBASIC,TOXICODENDRON RADICANS LEAF,HYPERICUM PERFORATUMThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECREAMThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE6/8/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEThe Magni Group IncName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEATROPA BELLADONNA; CAPSICUM; CITRULLUS COLOCYNTHIS FRUIT PULP; HYPERICUM PERFORATUM; MAGNESIUM PHOSPHATE, DIBASIC; TOXICODENDRON RADICANS LEAFAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH3; 3; 3; 3; 3; 3 
ACTIVE INGRED UNIT[hp_X]/113g; [hp_X]/113g; [hp_X]/113g; [hp_X]/113g; [hp_X]/113g; [hp_X]/113g 
PHARM CLASSESAllergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vegetable Proteins [CS] 

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This page was last updated on: 2/1/2023