Bulbinum 4ch
Oryctolagus Cuniculus (rabbit) Medulla Oblongata
Seroyal Usa
Human Otc Drug
NDC 62106-0244Bulbinum 4ch also known as Oryctolagus Cuniculus (rabbit) Medulla Oblongata is a human otc drug labeled by 'Seroyal Usa'. National Drug Code (NDC) number for Bulbinum 4ch is 62106-0244. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Bulbinum 4ch drug includes Oryctolagus Cuniculus Whole - 4 [hp_C]/30mL . The currest status of Bulbinum 4ch drug is Active.
Drug Information:
| Drug NDC: | 62106-0244 |
| 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: | Bulbinum 4ch |
| 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: | Oryctolagus Cuniculus (rabbit) Medulla Oblongata |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Seroyal Usa |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Liquid |
| 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: | ORYCTOLAGUS CUNICULUS WHOLE - 4 [hp_C]/30mL
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | ORAL
|
| 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: | 10 Feb, 2015 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 24 Dec, 2025 |
| 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: | Seroyal USA
|
| 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. |
| UPC: | 0883196324507
|
| UPC stands for Universal Product Code. |
| UNII: | 768BE616L8
|
| 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 |
|---|
| 62106-0244-0 | 30 mL in 1 BOTTLE, GLASS (62106-0244-0) | 10 Feb, 2015 | 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:
Indications helps maintain normal heart and respiratory function.
Product Elements:
Bulbinum 4ch oryctolagus cuniculus (rabbit) medulla oblongata oryctolagus cuniculus whole oryctolagus cuniculus whole alcohol water
Indications and Usage:
Indications helps maintain normal heart and respiratory function. directions adults and children (over 12 years): take 10 drops two to three times daily. children (1-12 years): take three to five drops two to three times daily. take for three weeks, then one week off and three weeks on for three months or as recommended by your healthcare practitioner. evaluate after three months. do not use if seel is missing or broken. store in a cool dry place.
Warnings:
Warnings if pregnant or breastfeeding, ask a healthcare professional before use. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away. if symptoms persist or worsen, consult your healthcare practitioner.
Dosage and Administration:
Directions adults and children (over 12 years): take 10 drops two to three times daily. children (1-12 years): take three to five drops two to three times daily. take for three weeks, then one week off and three weeks on for three months or as recommended by your healthcare practitioner. evaluate after three months. do not use if seel is missing or broken. store in a cool dry place.
Overdosage:
In case of overdose, get medical help or contact a poison control center right away.
Package Label Principal Display Panel:
Unda ndc 62106-0244-0 bulbinum 4ch homeopathic remedy contains 30% alcohol 1 fl oz (30 ml) 62106-0244