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NDC 82969-2172 Bestmade Natural Products Bm172

Aurum Iod,Belladonna,Guiacum,Hepar Sulp,Iodium,Laurocerasus,Phytolacca Dec Liquid Oral - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 82969-2172?
  5. Bestmade Natural Products Bm172 Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes

Product Information

Get all the details for National Drug Code (NDC) 82969-2172 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:
82969-2172
Proprietary Name:
Bestmade Natural Products Bm172
Non-Proprietary Name: [1]
Aurum Iod, Belladonna, Guiacum, Hepar Sulp, Iodium, Laurocerasus, Phytolacca Dec
Substance Name: [2]
Atropa Belladonna; Calcium Sulfide; Gold Monoiodide; Guaiacum Officinale Resin; Iodine; Phytolacca Americana Root; Prunus Laurocerasus Leaf
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
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 Name: [5]
Bestmade Natural Products
Labeler Code:
82969
Product Label ID:
2e7d1eee-9290-17e0-e063-6394a90a9eb8
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
01-01-2015
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - CLEAR LIQUID)
Size(s):
30 MM
Score:
1
Flavor(s):
MINT (C73404 - TASTELESS LIQUID)

Code Structure Chart

Product Details

What is NDC 82969-2172?

The NDC code 82969-2172 is assigned by the FDA to the product Bestmade Natural Products Bm172 which is a human over the counter drug product labeled by Bestmade Natural Products. The generic name of Bestmade Natural Products Bm172 is aurum iod, belladonna, guiacum, hepar sulp, iodium, laurocerasus, phytolacca dec. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 82969-2172-1 30 [hp_c] in 1 bottle, glass . 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 Bestmade Natural Products Bm172?

UsesTemporarily relieves occasional tonsil discomfort, throat discomfort, difficulty eating and swallowing, ear discomfort, elevated body temperature, chills, enlarged and irritated tonsils, and a rise in the body temperature.**CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE. NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.This product is not intended to diagnose, treat, cure, or prevent any disease.

What are Bestmade Natural Products Bm172 Active Ingredients?

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.

Which are Bestmade Natural Products Bm172 UNII Codes?

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

Which are Bestmade Natural Products Bm172 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

[1] 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.

[2] 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.

[3] 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[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".