85946-0001 NDC - CELL WELL (CALCIUM CARBONICA,CALCIUM FLUORATUM,CALCIUM PHOSPHORICUM,CALCIUM SULPHURICUM,FERRUM PHOSPHORICUM,KALIUM MURIATICUM,KALIUM PHOSPHORICUM,KALIUM SULPHURICUM,MAGNESIUM CARBONICA,MAGNESIUM PHOSPHORICUM,NATRUM MURIATICUM,NATRUM PHOSPHORICUM,NATRUM SULPHURICUM,SILICEA)

Drug Information

  • Product NDC: 85946-0001
  • Proprietary Name: Cell Well
  • Non Proprietary Name: Calcium Carbonica,Calcium Fluoratum,Calcium Phosphoricum,Calcium Sulphuricum,Ferrum Phosphoricum,Kalium Muriaticum,Kalium Phosphoricum,Kalium Sulphuricum,Magnesium Carbonica,Magnesium Phosphoricum,Natrum Muriaticum,Natrum Phosphoricum,Natrum Sulphuricum,Silicea
  • Active Ingredient(s): 6 [hp_X]/60mL CALCIUM FLUORIDE; 6 [hp_X]/60mL CALCIUM PHOSPHATE, UNSPECIFIED FORM; 6 [hp_X]/60mL CALCIUM SULFATE, UNSPECIFIED FORM; 6 [hp_X]/60mL FERROSOFERRIC PHOSPHATE; 6 [hp_X]/60mL MAGNESIUM CARBONATE; 6 [hp_X]/60mL MAGNESIUM PHOSPHATE ANHYDROUS; 6 [hp_X]/60mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 6 [hp_X]/60mL POTASSIUM CHLORIDE; 6 [hp_X]/60mL POTASSIUM PHOSPHATE, UNSPECIFIED FORM; 6 [hp_X]/60mL POTASSIUM SULFATE; 6 [hp_Q]/60mL SILICON DIOXIDE; 6 [hp_X]/60mL SODIUM CHLORIDE; 6 [hp_Q]/60mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; 6 [hp_X]/60mL SODIUM SULFATE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Blood Coagulation Factor [EPC]; Blood Coagulation Factor [EPC]; Calcium [CS]; Calcium [CS]; Cations; Divalent [CS]; Cations; Divalent [CS]; Increased Coagulation Factor Activity [PE]; Increased Coagulation Factor Activity [PE]; Increased Large Intestinal Motility [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Osmotic Laxative [EPC]; Phosphate Binder [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Phosphate Chelating Activity [MoA]; Potassium Compounds [CS]; Potassium Compounds [CS]; Potassium Salt [EPC]; Potassium Salt [EPC]

Labeler Information

Field Name Field Value
Labeler Name: JoyWell Co LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:11/19/2025

Package Information

No. Package Code Package Description Billing Unit
185946-0001-160 mL in 1 BOTTLE, DROPPER (85946-0001-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC85946-0001The 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 NAMECell WellThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECalcium Carbonica,Calcium Fluoratum,Calcium Phosphoricum,Calcium Sulphuricum,Ferrum Phosphoricum,Kalium Muriaticum,Kalium Phosphoricum,Kalium Sulphuricum,Magnesium Carbonica,Magnesium Phosphoricum,Natrum Muriaticum,Natrum Phosphoricum,Natrum Sulphuricum,SiliceaThe 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 DATE11/19/2025This 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 NAMEJoyWell Co LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECALCIUM FLUORIDE; CALCIUM PHOSPHATE, UNSPECIFIED FORM; CALCIUM SULFATE, UNSPECIFIED FORM; FERROSOFERRIC PHOSPHATE; MAGNESIUM CARBONATE; MAGNESIUM PHOSPHATE ANHYDROUS; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, UNSPECIFIED FORM; POTASSIUM SULFATE; SILICON DIOXIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM SULFATEAn 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 STRENGTH6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6 
ACTIVE INGRED UNIT[hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_Q]/60mL; [hp_X]/60mL; [hp_Q]/60mL; [hp_X]/60mL 
PHARM CLASSESBlood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Calcium [CS], Calcium [CS], Cations, Divalent [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Compounds [CS], Potassium Salt [EPC], Potassium Salt [EPC] 

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This page was last updated on: 12/19/2025

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