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  4. NDC Product Code: 62795-2004 Bodyanew

NDC 62795-2004 Bodyanew

View Dosage, Usage, Ingredients, Routes, UNII

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.

Get all the details for National Drug Code (NDC) 62795-2004 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:
62795-2004
Proprietary Name:
Bodyanew
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
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.
Start Marketing Date: [9]
01-01-2018
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 62795-2004?

The NDC code 62795-2004 is assigned by the FDA to the product Bodyanew which is product labeled by Medinatura Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62795-2004-4 1 kit in 1 kit * 50 ml in 1 bottle (62795-2007-4) * 50 ml in 1 bottle (62795-2009-4) * 50 ml in 1 bottle (62795-2008-4). 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 Bodyanew?

For the temporary relief of occasional low energy, minor abdominal bloating, upper respiratory symtoms such as cough, runny nose, urinary pain.

Which are Bodyanew 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 Bodyanew 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:

* Please review the disclaimer below.

Product Footnotes

[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".