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NDC 81403-0001 2 Transform

Fucus Vesiculosus,Chelidonium Majus,Kali Phosphoricum,Lycopodium Clavatum,Natrum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81403-0001?
  4. 2 Transform Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 81403-0001 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
81403-0001
Proprietary Name:
2 Transform
Non-Proprietary Name: [1]
Fucus Vesiculosus, Chelidonium Majus, Kali Phosphoricum, Lycopodium Clavatum, Natrum Muriaticum, Quercus Glandium Spiritus, Quercus Robur, Nux Vomica, Phytolacca Decandra, Ornithogalum Umbellatum, Agnus Castus, Berberis Aquifolium, Berberis Vulgaris, Saccharum Officinale, Solidago Virgaurea, Calcarea Carbonica, Carbo Vegetabilis, Magnesia Phosphorica, Natrum Phosphoricum, Sinapis Arvensis, Flos, Ubidecarenonum, Graphites, Hypophysis Suis, Placenta Totalis Suis, Hypothalamus (bovine)
Substance Name: [2]
Activated Charcoal; Berberis Aquifolium Root Bark; Berberis Vulgaris Root Bark; Bos Taurus Hypothalamus; Chaste Tree Fruit; Chelidonium Majus Whole; Dibasic Potassium Phosphate; Fucus Vesiculosus; Graphite; Lycopodium Clavatum Spore; Magnesium Phosphate, Dibasic Trihydrate; Ornithogalum Umbellatum Whole; Oyster Shell Calcium Carbonate, Crude; Phytolacca Americana Root; Quercus Robur Nut; Quercus Robur Twig Bark; Sinapis Arvensis Flowering/fruiting Top; Sodium Chloride; Sodium Phosphate, Dibasic, Heptahydrate; Solidago Virgaurea Flowering Top; Strychnos Nux-vomica Seed; Sucrose; Sus Scrofa Pituitary Gland; Sus Scrofa Placenta; Ubidecarenone
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]
Murphree Chiropractic
Labeler Code:
81403
Product Label ID:
64e50164-a888-42bc-aec3-7c93909c4787
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
06-28-2021
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 81403-0001?

The NDC code 81403-0001 is assigned by the FDA to the product 2 Transform which is a human over the counter drug product labeled by Murphree Chiropractic. The generic name of 2 Transform is fucus vesiculosus, chelidonium majus, kali phosphoricum, lycopodium clavatum, natrum muriaticum, quercus glandium spiritus, quercus robur, nux vomica, phytolacca decandra, ornithogalum umbellatum, agnus castus, berberis aquifolium, berberis vulgaris, saccharum officinale, solidago virgaurea, calcarea carbonica, carbo vegetabilis, magnesia phosphorica, natrum phosphoricum, sinapis arvensis, flos, ubidecarenonum, graphites, hypophysis suis, placenta totalis suis, hypothalamus (bovine). 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 81403-0001-1 60 ml in 1 bottle, dropper . 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 2 Transform?

For weight management and inflammation support.This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective. For weight management and inflammation support.This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

What are 2 Transform 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 2 Transform UNII Codes?

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

  • FUCUS VESICULOSUS (UNII: 535G2ABX9M)
  • FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
  • CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN)
  • CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
  • DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
  • PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
  • QUERCUS ROBUR NUT (UNII: Q7MU1F4GLY)
  • QUERCUS ROBUR NUT (UNII: Q7MU1F4GLY) (Active Moiety)
  • QUERCUS ROBUR TWIG BARK (UNII: 2JFK226947)
  • QUERCUS ROBUR TWIG BARK (UNII: 2JFK226947) (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)
  • ORNITHOGALUM UMBELLATUM WHOLE (UNII: 9NS3M2Y78S)
  • ORNITHOGALUM UMBELLATUM (UNII: 9NS3M2Y78S) (Active Moiety)
  • CHASTE TREE FRUIT (UNII: 433OSF3U8A)
  • CHASTE TREE (UNII: 433OSF3U8A) (Active Moiety)
  • BERBERIS AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB)
  • BERBERIS AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • SUCROSE (UNII: C151H8M554)
  • SUCROSE (UNII: C151H8M554) (Active Moiety)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
  • ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
  • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
  • SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
  • SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK)
  • SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK) (Active Moiety)
  • UBIDECARENONE (UNII: EJ27X76M46)
  • UBIDECARENONE (UNII: EJ27X76M46) (Active Moiety)
  • GRAPHITE (UNII: 4QQN74LH4O)
  • GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
  • SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT)
  • SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT) (Active Moiety)
  • SUS SCROFA PLACENTA (UNII: C8CV8867O8)
  • SUS SCROFA PLACENTA (UNII: C8CV8867O8) (Active Moiety)
  • BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7)
  • BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7) (Active Moiety)

Which are 2 Transform 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 2 Transform?

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.

* 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, 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".