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  4. NDC Product Code: 55714-4786 Mega Menses

NDC 55714-4786 Mega Menses

Apis Mellifica,Hamamelis Virginiana,Hydrastis Canadensis,Aletris Farinosa,Apocynum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 55714-4786?
  4. Mega Menses Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
55714-4786
Proprietary Name:
Mega Menses
Non-Proprietary Name: [1]
Apis Mellifica, Hamamelis Virginiana, Hydrastis Canadensis, Aletris Farinosa, Apocynum Cannabinum, Cinchona Officinalis, Cinnamomum, Conium Maculatum, Helonias Dioica, Lilium Tigrinum, Millefolium, Phosphorus, Secale Cornutum, Thlaspi Bursa-pastoris, Trillium Pendulum.
Substance Name: [2]
Achillea Millefolium; Aletris Farinosa Root; Apis Mellifera; Apocynum Cannabinum Root; Capsella Bursa-pastoris; Chamaelirium Luteum Root; Cinchona Officinalis Bark; Cinnamon; Claviceps Purpurea Sclerotium; Conium Maculatum Flowering Top; Goldenseal; Hamamelis Virginiana Root Bark/stem Bark; Lilium Lancifolium Whole Flowering; Phosphorus; Trillium Erectum Root
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Newton Laboratories, Inc.
    Labeler Code:
    55714
    Product Label ID:
    9a646b7e-23dd-c2e5-e053-2995a90a66c1
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    09-02-2019
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 55714-4786?

    The NDC code 55714-4786 is assigned by the FDA to the product Mega Menses which is a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Mega Menses is apis mellifica, hamamelis virginiana, hydrastis canadensis, aletris farinosa, apocynum cannabinum, cinchona officinalis, cinnamomum, conium maculatum, helonias dioica, lilium tigrinum, millefolium, phosphorus, secale cornutum, thlaspi bursa-pastoris, trillium pendulum.. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 55714-4786-1 30 ml in 1 bottle, glass . 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 Mega Menses?

    Formulated for symptoms such as prolonged or heavy menses and pelvic pain.

    What are Mega Menses 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 Mega Menses UNII Codes?

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

    • APIS MELLIFERA (UNII: 7S82P3R43Z)
    • APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
    • CAPSELLA BURSA-PASTORIS (UNII: W0X9457M59)
    • CAPSELLA BURSA-PASTORIS (UNII: W0X9457M59) (Active Moiety)
    • GOLDENSEAL (UNII: ZW3Z11D0JV)
    • GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
    • ALETRIS FARINOSA ROOT (UNII: O021JGR97X)
    • ALETRIS FARINOSA ROOT (UNII: O021JGR97X) (Active Moiety)
    • APOCYNUM CANNABINUM ROOT (UNII: 2F92409L9Z)
    • APOCYNUM CANNABINUM ROOT (UNII: 2F92409L9Z) (Active Moiety)
    • CINCHONA OFFICINALIS BARK (UNII: S003A158SB)
    • CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (Active Moiety)
    • CINNAMON (UNII: 5S29HWU6QB)
    • CINNAMON (UNII: 5S29HWU6QB) (Active Moiety)
    • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
    • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
    • CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U)
    • CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U) (Active Moiety)
    • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI)
    • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (Active Moiety)
    • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
    • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
    • PHOSPHORUS (UNII: 27YLU75U4W)
    • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
    • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
    • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
    • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
    • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
    • TRILLIUM ERECTUM ROOT (UNII: AHW6F0T2X0)
    • TRILLIUM ERECTUM ROOT (UNII: AHW6F0T2X0) (Active Moiety)

    Which are Mega Menses 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 Mega Menses?

    * 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".