NDC 82969-7100 Bestmade Natural Products Bm100 Pellets

Agraphis Nutans,Castoreum,Formica Rufa,Lemna Minor,Sanguinaria Nitricum,Sticta - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

Get all the details for National Drug Code (NDC) 82969-7100 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:
82969-7100
Proprietary Name:
Bestmade Natural Products Bm100 Pellets
Non-Proprietary Name: [1]
Agraphis Nutans, Castoreum, Formica Rufa, Lemna Minor, Sanguinaria Nitricum, Sticta Pul, Teucrium Marum, Thuja
Substance Name: [2]
Castor Fiber Scent Gland Secretion; Formica Rufa; Hyacinthoides Non-scripta Whole; Lemna Minor Whole; Lobaria Pulmonaria; Sanguinarine Nitrate; Teucrium Marum Whole; Thuja Occidentalis Leafy Twig
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet, Soluble - A solid dosage form that contains medicinal substances with or without suitable diluents and possesses the ability to dissolve in fluids.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Code:
82969
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 - WHITE DISSOLVABLE TABLETS)
Shape:
ROUND (C48348)
Size(s):
90 MM
Score:
1

Code Structure Chart

Product Details

What is NDC 82969-7100?

The NDC code 82969-7100 is assigned by the FDA to the product Bestmade Natural Products Bm100 Pellets which is a human over the counter drug product labeled by Bestmade Natural Products. The generic name of Bestmade Natural Products Bm100 Pellets is agraphis nutans, castoreum, formica rufa, lemna minor, sanguinaria nitricum, sticta pul, teucrium marum, thuja. The product's dosage form is tablet, soluble and is administered via oral form. The product is distributed in a single package with assigned NDC code 82969-7100-1 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 Bm100 Pellets?

UsesTemporarily relieves occasional nasal obstruction and discomfort, swelling and irritation of the lining of the nose, sneezing, poor sense of smell and taste, and catarrh.* *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 Bm100 Pellets 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 Bm100 Pellets UNII Codes?

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

  • FORMICA RUFA (UNII: 55H0W83JO5)
  • FORMICA RUFA (UNII: 55H0W83JO5) (Active Moiety)
  • TEUCRIUM MARUM WHOLE (UNII: 10464S0TAA)
  • TEUCRIUM MARUM WHOLE (UNII: 10464S0TAA) (Active Moiety)
  • SANGUINARINE NITRATE (UNII: BOP122S791)
  • NITRATE ION (UNII: T93E9Y2844) (Active Moiety)
  • LOBARIA PULMONARIA (UNII: D1YM0P5Z2T)
  • LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (Active Moiety)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
  • HYACINTHOIDES NON-SCRIPTA WHOLE (UNII: 5F658PFU56)
  • HYACINTHOIDES NON-SCRIPTA WHOLE (UNII: 5F658PFU56) (Active Moiety)
  • CASTOR FIBER SCENT GLAND SECRETION (UNII: 9X8XFD5ZQX)
  • CASTOR FIBER SCENT GLAND SECRETION (UNII: 9X8XFD5ZQX) (Active Moiety)
  • LEMNA MINOR WHOLE (UNII: 621HHM46SV)
  • LEMNA MINOR WHOLE (UNII: 621HHM46SV) (Active Moiety)

Which are Bestmade Natural Products Bm100 Pellets 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".