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NDC 69676-0045 Genexa Leg Cramps

Angustura Vera,Berberis Vulgaris,Chamomilla,Colchicum Autumnale,Colocynthis,Ignatia - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69676-0045?
  5. Genexa Leg Cramps Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

NDC Product Code:
69676-0045
Proprietary Name:
Genexa Leg Cramps
Non-Proprietary Name: [1]
Angustura Vera, Berberis Vulgaris, Chamomilla, Colchicum Autumnale, Colocynthis, Ignatia Amara, Jatropha Curcas, Lycopodium Clavatum, Nux Moshchata, Rhus Toxicodendron, Secale Cornutum, Veratrum Album
Substance Name: [2]
Angostura Bark; Berberis Vulgaris Root Bark; Citrullus Colocynthis Fruit Pulp; Claviceps Purpurea Sclerotium; Colchicum Autumnale Bulb; Jatropha Curcas Seed; Lycopodium Clavatum Spore; Matricaria Chamomilla; Nutmeg; Strychnos Ignatii Seed; Toxicodendron Pubescens Leaf; Veratrum Album Root
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Genexa Inc.
    Labeler Code:
    69676
    Product Label ID:
    b012df58-15fb-5c73-e053-2995a90a9d2b
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    09-15-2020
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Characteristics

    Color(s):
    WHITE (C48325 - OFF-WHITE)
    Shape:
    ROUND (C48348)
    Size(s):
    10 MM
    Imprint(s):
    G
    Score:
    1
    Flavor(s):
    GRAPE (C73391)

    Product Packages

    NDC Code 69676-0045-2

    Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

    Product Details

    What is NDC 69676-0045?

    The NDC code 69676-0045 is assigned by the FDA to the product Genexa Leg Cramps which is a human over the counter drug product labeled by Genexa Inc.. The generic name of Genexa Leg Cramps is angustura vera, berberis vulgaris, chamomilla, colchicum autumnale, colocynthis, ignatia amara, jatropha curcas, lycopodium clavatum, nux moshchata, rhus toxicodendron, secale cornutum, veratrum album. The product's dosage form is tablet, chewable and is administered via oral form. The product is distributed in a single package with assigned NDC code 69676-0045-2 1 bottle, plastic in 1 carton / 100 tablet, chewable in 1 bottle, plastic. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Genexa Leg Cramps?

    Uses*addresses stiffness, pain in limbs, joints, and legs, and cramps in calves, feet and legs.

    What are Genexa Leg Cramps Active Ingredients?

    An 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.

    Which are Genexa Leg Cramps UNII Codes?

    The UNII codes for the active ingredients in this product are:

    • MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)
    • MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (Active Moiety)
    • ANGOSTURA BARK (UNII: 104010O5VU)
    • ANGOSTURA BARK (UNII: 104010O5VU) (Active Moiety)
    • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
    • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
    • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
    • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
    • STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
    • STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
    • JATROPHA CURCAS SEED (UNII: J0F5GM8LA8)
    • JATROPHA CURCAS SEED (UNII: J0F5GM8LA8) (Active Moiety)
    • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
    • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
    • NUTMEG (UNII: AEE24M3MQ9)
    • NUTMEG (UNII: AEE24M3MQ9) (Active Moiety)
    • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
    • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
    • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
    • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
    • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
    • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)
    • COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
    • COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)

    Which are Genexa Leg Cramps Inactive Ingredients UNII Codes?

    The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

    Which are the Pharmacologic Classes for Genexa Leg Cramps?

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An 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.

    [3] What kind of product is this? - Indicates 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] What is the Marketing Category? - Product 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".