Bodyanew
NDC 62795-2004

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 62795-2004?
  4. Bodyanew 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 inactivated by the FDA.

Bodyanew is a UNAPPROVED HOMEOPATHIC-approved product labeled by Medinatura Inc. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 62795-2004 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
62795-2004
Proprietary Name:
Bodyanew
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Medinatura Inc
Labeler Code:
62795
Product Label ID:
e5f86823-624d-44a6-830f-2d5c7187fdef
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
01-01-2018
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 62795-2004?

The NDC code 62795-2004 is assigned by the FDA to the product Bodyanew. This pharmaceutical product is labeled by Medinatura Inc 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: 62795-2004-4. 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 the temporary relief of occasional low energy, minor abdominal bloating, upper respiratory symtoms such as cough, runny nose, urinary pain.

Which are the associated UNII Codes?

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

  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
  • CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
  • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
  • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)
  • APIS MELLIFERA (UNII: 7S82P3R43Z)
  • APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
  • TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
  • CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
  • SOLANUM DULCAMARA TOP (UNII: KPS1B1162N)
  • SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (Active Moiety)
  • EQUISETUM HYEMALE (UNII: 59677RXH25)
  • EQUISETUM HYEMALE (UNII: 59677RXH25) (Active Moiety)
  • FERROUS IODIDE (UNII: F5452U54PN)
  • FERROUS IODIDE (UNII: F5452U54PN) (Active Moiety)
  • FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL)
  • FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL) (Active Moiety)
  • GENTIANA LUTEA ROOT (UNII: S72O3284MS)
  • GENTIANA LUTEA ROOT (UNII: S72O3284MS) (Active Moiety)
  • GERANIUM ROBERTIANUM (UNII: R5I1HK0UBL)
  • GERANIUM ROBERTIANUM (UNII: R5I1HK0UBL) (Active Moiety)
  • POTASSIUM IODIDE (UNII: 1C4QK22F9J)
  • IODIDE ION (UNII: 09G4I6V86Q) (Active Moiety)
  • SODIUM SULFATE (UNII: 0YPR65R21J)
  • SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
  • PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73)
  • PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73) (Active Moiety)
  • SMILAX REGELII ROOT (UNII: 2H1576D5WG)
  • SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
  • SCROPHULARIA NODOSA (UNII: 7H443NUB2T)
  • SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (Active Moiety)
  • LOBARIA PULMONARIA (UNII: D1YM0P5Z2T)
  • LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (Active Moiety)
  • TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G)
  • TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G) (Active Moiety)
  • VERONICA OFFICINALIS FLOWERING TOP (UNII: 9IH82J936J)
  • VERONICA OFFICINALIS FLOWERING TOP (UNII: 9IH82J936J) (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 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".