NDC 73253-0001 Mfl 20/40
Asclepias Vincetoxicum,Echinacea (angustifolia),Hypothalamus (suis),Cerebrum Suis,Hepar - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 73253-0001?
What are the uses for Mfl 20/40?
What are Mfl 20/40 Active Ingredients?
- 7-OXODEHYDROEPIANDROSTERONE 3-ACETATE 30 [hp_X]/mL
- ADENOSINE TRIPHOSPHATE DISODIUM 30 [hp_X]/mL
- APC-356433 8 [hp_X]/mL
- APC-356434 8 [hp_X]/mL
- CYNANCHUM VINCETOXICUM ROOT 6 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA 6 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- GAMBOGE 14 [hp_X]/mL - A plant genus of the family CLUSIACEAE. Members contain XANTHONES.
- GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X]/mL
- GRAPHITE 12 [hp_X]/mL - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
- INSULIN PORK 30 [hp_X]/mL
- LACTIC ACID, L- 30 [hp_X]/mL
- METHYLCOBALAMIN 8 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 12 [hp_X]/mL
- PORK KIDNEY 8 [hp_X]/mL
- PORK LIVER 8 [hp_X]/mL
- PROTEUS VULGARIS 30 [hp_C]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that occurs in soil, fecal matter, and sewage. It is an opportunistic pathogen and causes cystitis and pyelonephritis.
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
- SUS SCROFA CEREBRUM 8 [hp_X]/mL
- SUS SCROFA HYPOTHALAMUS 6 [hp_X]/mL
- SUS SCROFA PANCREAS 8 [hp_X]/mL
- SUS SCROFA STOMACH 8 [hp_X]/mL
Which are Mfl 20/40 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CYNANCHUM VINCETOXICUM ROOT (UNII: 9R858U917W)
- CYNANCHUM VINCETOXICUM ROOT (UNII: 9R858U917W) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (Active Moiety)
- SUS SCROFA CEREBRUM (UNII: 4GB5DQR532)
- SUS SCROFA CEREBRUM (UNII: 4GB5DQR532) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- PORK KIDNEY (UNII: X7BCI5P86H)
- PORK KIDNEY (UNII: X7BCI5P86H) (Active Moiety)
- METHYLCOBALAMIN (UNII: BR1SN1JS2W)
- METHYLCOBALAMIN (UNII: BR1SN1JS2W) (Active Moiety)
- SUS SCROFA PANCREAS (UNII: 9Y3J3362RY)
- SUS SCROFA PANCREAS (UNII: 9Y3J3362RY) (Active Moiety)
- SUS SCROFA STOMACH (UNII: T0920P9Z9A)
- SUS SCROFA STOMACH (UNII: T0920P9Z9A) (Active Moiety)
- APC-356433 (UNII: TX3FV9N212)
- APC-356433 (UNII: TX3FV9N212) (Active Moiety)
- APC-356434 (UNII: NN413ZO15B)
- APC-356434 (UNII: NN413ZO15B) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- GAMBOGE (UNII: 7556HJ7587)
- GAMBOGE (UNII: 7556HJ7587) (Active Moiety)
- 7-OXODEHYDROEPIANDROSTERONE 3-ACETATE (UNII: 84RQ0XOM11)
- 7-OXODEHYDROEPIANDROSTERONE 3-ACETATE (UNII: 84RQ0XOM11) (Active Moiety)
- ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE) (Active Moiety)
- INSULIN PORK (UNII: AVT680JB39)
- INSULIN PORK (UNII: AVT680JB39) (Active Moiety)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- PROTEUS VULGARIS (UNII: 11T9HCO30O)
- PROTEUS VULGARIS (UNII: 11T9HCO30O) (Active Moiety)
Which are Mfl 20/40 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Mfl 20/40?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
* Please review the disclaimer below.
[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.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[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".