NDC 73253-0001 Mfl 20/40

Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Cerebrum Suis, Hepar Suis, Kidney (suis), Methylcobalamin, Pancreas Suis, Stomach (suis), Aacg-a, Aacg-b, Calcarea Carbonica, Gelsemium Sempervirens, Graphites, Nux Vomica, Phytolacca Decandra, Gambogia, 7-oxo-dehydroepiandrosterone 3-acetate, Adenosinum Triphosphoricum Dinatrum, Insulinum (suis), Sarcolacticum Acidum, Proteus (vulgaris)

NDC Product Code 73253-0001

NDC Code: 73253-0001

Proprietary Name: Mfl 20/40 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.

Non-Proprietary Name: Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Cerebrum Suis, Hepar Suis, Kidney (suis), Methylcobalamin, Pancreas Suis, Stomach (suis), Aacg-a, Aacg-b, Calcarea Carbonica, Gelsemium Sempervirens, Graphites, Nux Vomica, Phytolacca Decandra, Gambogia, 7-oxo-dehydroepiandrosterone 3-acetate, Adenosinum Triphosphoricum Dinatrum, Insulinum (suis), Sarcolacticum Acidum, Proteus (vulgaris) 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.

NDC Code Structure

NDC 73253-0001-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Mfl 20/40 with NDC 73253-0001 is a a human over the counter drug product labeled by Mass Fatloss Com. The generic name of Mfl 20/40 is asclepias vincetoxicum, echinacea (angustifolia), hypothalamus (suis), cerebrum suis, hepar suis, kidney (suis), methylcobalamin, pancreas suis, stomach (suis), aacg-a, aacg-b, calcarea carbonica, gelsemium sempervirens, graphites, nux vomica, phytolacca decandra, gambogia, 7-oxo-dehydroepiandrosterone 3-acetate, adenosinum triphosphoricum dinatrum, insulinum (suis), sarcolacticum acidum, proteus (vulgaris). The product's dosage form is liquid and is administered via oral form.

Labeler Name: Mass Fatloss Com

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.

Product Type: Human Otc Drug 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.

Mfl 20/40 Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • CYNANCHUM VINCETOXICUM ROOT 6 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 6 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS 6 [hp_X]/mL
  • SUS SCROFA CEREBRUM 8 [hp_X]/mL
  • PORK LIVER 8 [hp_X]/mL
  • PORK KIDNEY 8 [hp_X]/mL
  • METHYLCOBALAMIN 8 [hp_X]/mL
  • SUS SCROFA PANCREAS 8 [hp_X]/mL
  • SUS SCROFA STOMACH 8 [hp_X]/mL
  • APC-356433 8 [hp_X]/mL
  • APC-356434 8 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X]/mL
  • GRAPHITE 12 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 12 [hp_X]/mL
  • GAMBOGE 14 [hp_X]/mL
  • 7-OXODEHYDROEPIANDROSTERONE 3-ACETATE 30 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 30 [hp_X]/mL
  • INSULIN PORK 30 [hp_X]/mL
  • LACTIC ACID, L- 30 [hp_X]/mL
  • PROTEUS VULGARIS 30 [hp_C]/mL

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.

Labeler Name: Mass Fatloss Com
Labeler Code: 73253
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 10-10-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Mfl 20/40 Product Label Images