NDC 82969-6016 Bestmade Natural Products Daily Wellness - Be-rubia

Calcarea Carbonica,Calcarea Iodata,Calcarea Phosphorica,Ferrum Phosphoricum,Magnesia - View Dosage, Usage, Ingredients, Routes, UNII

Product Information
Product Packages
Product Characteristics
What is NDC 82969-6016?
Bestmade Natural Products Daily Wellness - Be-rubia Uses
Active Ingredients
Active Ingredients UNII Codes
Inactive Ingredients UNII Codes
Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 82969-6016 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:

82969-6016

Proprietary Name:

Bestmade Natural Products Daily Wellness - Be-rubia

Non-Proprietary Name: [1]

Calcarea Carbonica, Calcarea Iodata, Calcarea Phosphorica, Ferrum Phosphoricum, Magnesia Phosphorica, Natrum Phosphoricum, Natrum Sulphuricum, Silicea, Juglans Regia, Rubia Tinctoria

Substance Name: [2]

Calcium Iodide; Ferrosoferric Phosphate; Juglans Regia Flowering Top; Magnesium Phosphate, Dibasic Trihydrate; Oyster Shell Calcium Carbonate, Crude; Rubia Tinctorum Whole; Silica; Sodium Phosphate, Dibasic, Heptahydrate; Sodium Sulfate; Tribasic Calcium Phosphate

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:

29b50d5d-fb6c-a54c-e063-6294a90ab8cd

Marketing Category: [8]

UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Start Marketing Date: [9]

01-01-2025

Listing Expiration Date: [11]

12-31-2025

Exclude Flag: [12]

Code Navigator:

Product Characteristics

Color(s):

WHITE (C48325 - CLEAR LIQUID)

Size(s):

30 MM

Score:

Flavor(s):

MINT (C73404 - TASTELESS LIQUID)

Code Structure Chart

Product Details

What is NDC 82969-6016?

The NDC code 82969-6016 is assigned by the FDA to the product Bestmade Natural Products Daily Wellness - Be-rubia which is a human over the counter drug product labeled by Bestmade Natural Products. The generic name of Bestmade Natural Products Daily Wellness - Be-rubia is calcarea carbonica, calcarea iodata, calcarea phosphorica, ferrum phosphoricum, magnesia phosphorica, natrum phosphoricum, natrum sulphuricum, silicea, juglans regia, rubia tinctoria. 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 82969-6016-1 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 Daily Wellness - Be-rubia?

Traditionally used in homeopathy to support natural growth and overall well-being.

What are Bestmade Natural Products Daily Wellness - Be-rubia 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 Daily Wellness - Be-rubia UNII Codes?

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

MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
CALCIUM IODIDE (UNII: 8EKI9QEE2H)
CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
SILICA (UNII: ETJ7Z6XBU4)
SILICA (UNII: ETJ7Z6XBU4) (Active Moiety)
SODIUM SULFATE (UNII: 0YPR65R21J)
SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG)
JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG) (Active Moiety)
RUBIA TINCTORUM WHOLE (UNII: DEF14459OH)
RUBIA TINCTORUM WHOLE (UNII: DEF14459OH) (Active Moiety)

Which are Bestmade Natural Products Daily Wellness - Be-rubia 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:

ALCOHOL (UNII: 3K9958V90M)

Which are the Pharmacologic Classes for Bestmade Natural Products Daily Wellness - Be-rubia?

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.

* 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".

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