NDC 55714-4786 Mega Menses
Apis Mellifica, Hamamelis Virginiana, Hydrastis Canadensis, Aletris Farinosa, Apocynum...

Product Information

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, RxNorm crosswalk and the complete product label.

NDC Product Code55714-4786
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Mega Menses
Non-Proprietary Name 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.
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.
Product Type 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.
Human Otc Drug
Dosage FormLiquid - 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) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Newton Laboratories, Inc.
Labeler Code55714
Marketing Category 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.
UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
09-02-2019
Listing Expiration Date 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.
12-31-2023
Exclude Flag 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".
N
NDC Code Structure

What are the uses for Mega Menses?


Product Packages

NDC Code 55714-4786-1

Package Description: 30 mL in 1 BOTTLE, GLASS

Product Details

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.

Mega Menses Active Ingredients UNII Codes

  • 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)

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.

Pharmacologic Class(es)

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Mega Menses Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



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