2 Transform
NDC 81403-0001

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 81403-0001?
  4. 2 Transform Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

2 Transform is a UNAPPROVED HOMEOPATHIC-approved product labeled by Murphree Chiropractic. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 81403-0001 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
81403-0001
Proprietary Name:
2 Transform
Product Type: [3]
Code Navigator:

Labeler & Regulatory Data

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.

Marketing Timeline

Start Marketing Date: [9]
06-28-2021
End Marketing Date: [10]
08-12-2026
Listing Expiration Date: [11]
08-12-2026
Exclude Flag: [12]
D

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. This pharmaceutical product is labeled by Murphree Chiropractic and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 81403-0001-1. 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?

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.

Which are the associated 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 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:

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Product & Regulatory Definitions
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 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.
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".