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  4. NDC Product Code: 49726-042 Compulsin

NDC 49726-042 Compulsin

Calcarea Carbonica,Coffea Cruda,Iodium,Mancinella,Physostigma Venenosum,Silicea,Ulmus - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 49726-042?
  5. Compulsin Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

NDC Product Code:
49726-042
Proprietary Name:
Compulsin
Non-Proprietary Name: [1]
Calcarea Carbonica, Coffea Cruda, Iodium, Mancinella, Physostigma Venenosum, Silicea, Ulmus Procera, Flos
Substance Name: [2]
Arabica Coffee Bean; Hippomane Mancinella Fruiting Leafy Twig; Iodine; Oyster Shell Calcium Carbonate, Crude; Physostigma Venenosum Seed; Silicon Dioxide; Ulmus Minor Flowering Twig
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Hellolife, Inc.
    Labeler Code:
    49726
    Product Label ID:
    9c16d37c-43a4-406f-9156-9ab30f1b640c
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-15-2018
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Characteristics

    Color(s):
    WHITE (C48325)
    Shape:
    ROUND (C48348)
    Size(s):
    10 MM
    Imprint(s):
    H
    Score:
    1

    Code Structure Chart

    Product Details

    What is NDC 49726-042?

    The NDC code 49726-042 is assigned by the FDA to the product Compulsin which is a human over the counter drug product labeled by Hellolife, Inc.. The generic name of Compulsin is calcarea carbonica, coffea cruda, iodium, mancinella, physostigma venenosum, silicea, ulmus procera, flos. The product's dosage form is tablet and is administered via oral form. The product is distributed in a single package with assigned NDC code 49726-042-60 60 tablet 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 Compulsin?

    For the temporary relief of symptoms such as: • nervous, repetitive thoughts• disproportionate fears• nervous, repetitive behaviors• apprehensivenessProduct indications are based solely on Homeopathic Materia Medica and have not been evaluated by the FDA.

    What are Compulsin 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 Compulsin UNII Codes?

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

    • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
    • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
    • ARABICA COFFEE BEAN (UNII: 3SW678MX72)
    • ARABICA COFFEE BEAN (UNII: 3SW678MX72) (Active Moiety)
    • IODINE (UNII: 9679TC07X4)
    • IODINE (UNII: 9679TC07X4) (Active Moiety)
    • HIPPOMANE MANCINELLA FRUITING LEAFY TWIG (UNII: HU6EYI2I1W)
    • HIPPOMANE MANCINELLA FRUITING LEAFY TWIG (UNII: HU6EYI2I1W) (Active Moiety)
    • PHYSOSTIGMA VENENOSUM SEED (UNII: CJV9E9IIOA)
    • PHYSOSTIGMA VENENOSUM SEED (UNII: CJV9E9IIOA) (Active Moiety)
    • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
    • SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
    • ULMUS MINOR FLOWERING TWIG (UNII: J3O020I532)
    • ULMUS MINOR FLOWERING TWIG (UNII: J3O020I532) (Active Moiety)

    Which are Compulsin 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 Compulsin?

    * 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".