Bodyanew
Medinatura Inc
Human Otc Drug
NDC 62795-2004Bodyanew is a human otc drug labeled by 'Medinatura Inc'. National Drug Code (NDC) number for Bodyanew is 62795-2004. This drug is available in dosage form of Kit. The names of the active, medicinal ingredients in Bodyanew drug includes . The currest status of Bodyanew drug is Active.
Drug Information:
| Drug NDC: | 62795-2004 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Bodyanew |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Bodyanew |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Medinatura Inc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Kit |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | |
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | |
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 01 Jan, 2018 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 25 Jun, 2026 |
| 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. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | MediNatura Inc
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | |
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 62795-2004-4 | 1 KIT in 1 KIT (62795-2004-4) * 50 mL in 1 BOTTLE (62795-2008-4) * 50 mL in 1 BOTTLE (62795-2009-4) * 50 mL in 1 BOTTLE (62795-2007-4) | 01 Jan, 2018 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose for the temporary relief of occasional low energy, minor abdominal bloating, upper respiratory symtoms such as cough, runny nose, urinary pain.
Product Elements:
Bodyanew bodyanew bodyanew colon liver bryonia alba root, chelidonium majus, citrullus colocynthis fruit pulp, lycopodium clavatum spore, and strychnos nux-vomica seed bryonia alba root bryonia alba root chelidonium majus chelidonium majus citrullus colocynthis fruit pulp citrullus colocynthis fruit pulp lycopodium clavatum spore lycopodium clavatum spore strychnos nux-vomica seed strychnos nux-vomica seed alcohol water bodyanew kidney berberis vulgaris root bark, citrullus colocynthis fruit pulp, solidago virgaurea flowering top, and veratrum album root berberis vulgaris root bark berberis vulgaris root bark citrullus colocynthis fruit pulp citrullus colocynthis fruit pulp solidago virgaurea flowering top solidago virgaurea flowering top veratrum album root veratrum album root alcohol water bodyanew lymph lungs apis mellifera, tribasic calcium phosphate, solanum dulcamara top, equisetum hyemale, ferrous iodide, fumaria officinalis flowering top, gentiana lutea root, geranium robertianum, potassium iodide, nasturtium officinale, sodium sulfate, pinus sylvestris leafy twig, smilax regelii root, scrophularia nodosa, lobaria pulmonaria, teucrium scorodonia flowering top, and veronica officinalis flowering top apis mellifera apis mellifera tribasic calcium phosphate calcium cation solanum dulcamara top solanum dulcamara top equisetum hyemale equisetum hyemale ferrous iodide ferrous iodide fumaria officinalis flowering top fumaria officinalis flowering top gentiana lutea root gentiana lutea root geranium robertianum geranium robertianum potassium iodide iodide ion sodium sulfate sodium sulfate anhydrous pinus sylvestris leafy twig pinus sylvestris leafy twig smilax ornata root smilax ornata root scrophularia nodosa scrophularia nodosa lobaria pulmonaria lobaria pulmonaria teucrium scorodonia flowering top teucrium scorodonia flowering top veronica officinalis flowering top veronica officinalis flowering top alcohol water
Indications and Usage:
Indications and usage for the temporary relief of occasional low energy, minor abdominal bloating, upper respiratory symtoms such as cough, runny nose, urinary pain.
Warnings:
Warnings if pregnant or breast-feeding, ask a healthcare professsional before use. keep out of reach of children. do not use if known hypersensitivity to bodyanew colon & liverâ¢, bodyanew kidneyâ¢, or bodyanew lymph & lungs⢠or any of its ingredients exists. mild symptoms such as skin outbreaks, and loose stools may occur. stop and see a doctor if these symtoms persist.
Dosage and Administration:
Directions directions: use for up to 2 weeks. adults : add 30 drops or 2 half dropperfuls of each bodyanew⢠formula( lymph & lungs, kidney, colon & liver) to water and consume throughtout the day. do not exceed more than 4 half dropperfuls of each formula per day.perday, taking 10 drops every 4 to 6 hours. for children under 18 years: consult your health practitioner.
Package Label Principal Display Panel:
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