Mega Menses Liquid
NDC 55714-4786
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Mega Menses (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.) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Newton Laboratories, Inc.. This medication is typically used as a allergens [cs]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 55714-4786 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
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
Code Navigator:
Clinical Specifications
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 & Regulatory Data
Labeler Name: [5]
Labeler Code:
55714
Product Label ID:
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Marketing Timeline
Start Marketing Date: [9]
09-02-2019
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
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. It is commonly known by its generic name, 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.. This pharmaceutical product is labeled by Newton Laboratories, Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 55714-4786-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
Formulated for symptoms such as prolonged or heavy menses and pelvic pain.
What are Active Ingredients of this product?
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.
- ACHILLEA MILLEFOLIUM 15 [hp_X]/mL - A plant genus of the family ASTERACEAE that has long been used in folk medicine for treating wounds.
- ALETRIS FARINOSA ROOT 15 [hp_X]/mL
- APIS MELLIFERA 6 [hp_X]/mL
- APOCYNUM CANNABINUM ROOT 15 [hp_X]/mL
- CAPSELLA BURSA-PASTORIS 15 [hp_X]/mL - A plant genus of the family CRUCIFERAE.
- CHAMAELIRIUM LUTEUM ROOT 15 [hp_X]/mL
- CINCHONA OFFICINALIS BARK 15 [hp_X]/mL
- CINNAMON 15 [hp_X]/mL
- CLAVICEPS PURPUREA SCLEROTIUM 15 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP 15 [hp_X]/mL
- GOLDENSEAL 6 [hp_X]/mL
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 6 [hp_X]/mL
- LILIUM LANCIFOLIUM WHOLE FLOWERING 15 [hp_X]/mL
- PHOSPHORUS 15 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
- TRILLIUM ERECTUM ROOT 15 [hp_X]/mL
Which are the associated 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 the Inactive Ingredients associated 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes of this product?
A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.
- Allergens - [CS]
- Allergens - [CS]
- Bee Venoms - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
