Bestmade Natural Products Bm34 Liquid
NDC 82969-2034

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 82969-2034?
  5. Bestmade Natural Products Bm34 Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes
  9. Pharmacologic Classes

Product Information

Bestmade Natural Products Bm34 (aconited6, belladonnad5, bryoniad7, ferr phosd7, ipecacd7, lachesisd16, phosphorusd14) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Bestmade Natural Products. This medication is typically used as a iron [cs]. It is supplied as a white liquid for oral administration. This product entry covers the primary NDC 82969-2034 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
82969-2034
Proprietary Name:
Bestmade Natural Products Bm34
Non-Proprietary Name: [1]
Aconited6, Belladonnad5, Bryoniad7, Ferr Phosd7, Ipecacd7, Lachesisd16, Phosphorusd14
Substance Name: [2]
Aconitum Napellus; Atropa Belladonna; Bryonia Alba Root; Ferric Pyrophosphate; Ipecac; Lachesis Muta Venom; Phosphorus
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Bestmade Natural Products
Labeler Code:
82969
Product Label ID:
ef2cb539-05f5-8a71-e053-2a95a90a3ac5
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
01-01-2015
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Product Characteristics

Color(s):
WHITE (C48325 - CLEAR LIQUID)
Size(s):
30 MM
Score:
1
Flavor(s):

Code Structure Chart

Product Details

What is NDC 82969-2034?

The NDC code 82969-2034 is assigned by the FDA to the product Bestmade Natural Products Bm34. It is commonly known by its generic name, aconited6, belladonnad5, bryoniad7, ferr phosd7, ipecacd7, lachesisd16, phosphorusd14. This pharmaceutical product is labeled by Bestmade Natural Products and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 82969-2034-1. 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?

PRODUCT INFORMATION 30mL approximately a 1 month supply when used as recommended Formulated to: Help manage symptoms of pneumonia, including high fever and chills, muscle aches, and fatigue. It helps with a cough with or without sputum, sore throat, chest pain, and enlarged lymph glands in the neck.

What are Active Ingredients of this product?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
  • ACONITUM NAPELLUS 30 [hp_C]/30[hp_C] - A plant genus of the family RANUNCULACEAE. Members contain a number of diterpenoid alkaloids including: aconitans, hypaconitine, ACONITINE, jesaconitine, ignavine, napelline, and mesaconitine. The common name of Wolfbane is similar to the common name for ARNICA.
  • ATROPA BELLADONNA 30 [hp_C]/30[hp_C] - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
  • BRYONIA ALBA ROOT 30 [hp_C]/30[hp_C]
  • FERRIC PYROPHOSPHATE 30 [hp_C]/30[hp_C]
  • IPECAC 30 [hp_C]/30[hp_C] - A syrup made from the dried rhizomes of two different species, CEPHAELIS ipecacuanha and C. acuminata. They contain EMETINE, cephaeline, psychotrine and other ISOQUINOLINES. Ipecac syrup is used widely as an emetic acting both locally on the gastric mucosa and centrally on the chemoreceptor trigger zone.
  • LACHESIS MUTA VENOM 30 [hp_C]/30[hp_C]
  • PHOSPHORUS 30 [hp_C]/30[hp_C] - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.

Which are the associated UNII Codes?

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

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:

Which are the Pharmacologic Classes of this product?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What is the Substance Name? An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
What kind of product is this? Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
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".