82969-6016 NDC - BESTMADE NATURAL PRODUCTS DAILY WELLNESS - BE-RUBIA (CALCAREA CARBONICA, CALCAREA IODATA, CALCAREA PHOSPHORICA, FERRUM PHOSPHORICUM, MAGNESIA PHOSPHORICA, NATRUM PHOSPHORICUM, NATRUM SULPHURICUM, SILICEA, JUGLANS REGIA, RUBIA TINCTORIA)

Drug Information

  • Product NDC: 82969-6016
  • Proprietary Name: Bestmade Natural Products Daily Wellness - Be-Rubia
  • Non Proprietary Name: Calcarea Carbonica, Calcarea Iodata, Calcarea Phosphorica, Ferrum Phosphoricum, Magnesia Phosphorica, Natrum Phosphoricum, Natrum Sulphuricum, Silicea, Juglans Regia, Rubia Tinctoria
  • Active Ingredient(s): 30 [hp_C]/30[hp_C] CALCIUM IODIDE; 30 [hp_C]/30[hp_C] FERROSOFERRIC PHOSPHATE; 30 [hp_C]/30[hp_C] JUGLANS REGIA FLOWERING TOP; 30 [hp_C]/30[hp_C] MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; 30 [hp_C]/30[hp_C] OYSTER SHELL CALCIUM CARBONATE, CRUDE; 30 [hp_C]/30[hp_C] RUBIA TINCTORUM WHOLE; 30 [hp_C]/30[hp_C] SILICA; 30 [hp_C]/30[hp_C] SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; 30 [hp_C]/30[hp_C] SODIUM SULFATE; 30 [hp_C]/30[hp_C] TRIBASIC CALCIUM PHOSPHATE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Blood Coagulation Factor [EPC]; Calcium [CS]; Calculi Dissolution Agent [EPC]; Cations; Divalent [CS]; Increased Coagulation Factor Activity [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Labeler Information

Field Name Field Value
Labeler Name: Bestmade Natural Products
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:1/1/2025

Package Information

No. Package Code Package Description Billing Unit
182969-6016-130 [hp_C] in 1 BOTTLE, GLASS (82969-6016-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC82969-6016The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEBestmade Natural Products Daily Wellness - Be-RubiaThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECalcarea Carbonica, Calcarea Iodata, Calcarea Phosphorica, Ferrum Phosphoricum, Magnesia Phosphorica, Natrum Phosphoricum, Natrum Sulphuricum, Silicea, Juglans Regia, Rubia TinctoriaThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE1/1/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEBestmade Natural ProductsName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECALCIUM 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 PHOSPHATEAn 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.
ACTIVE NUMERATOR STRENGTH30; 30; 30; 30; 30; 30; 30; 30; 30; 30 
ACTIVE INGRED UNIT[hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C]; [hp_C]/30[hp_C] 
PHARM CLASSESBlood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] 

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This page was last updated on: 7/4/2025

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