64616-109 NDC - CAL-5-REVIVE (CALCIUM BALANCE)

Drug Information

Product NDC: 64616-109

Proprietary Name: Cal-5-Revive

Non Proprietary Name: Calcium Balance

Active Ingredient(s):
  • 20 [hp_X]/mL ACONITUM NAPELLUS;
  • 15 [hp_X]/mL BISMUTH SUBNITRATE;
  • 12 [hp_X]/mL CALCIUM ARSENATE;
  • 25 [hp_X]/mL CALCIUM FLUORIDE;
  • 27 [hp_X]/mL CALCIUM HYDROXIDE;
  • 10 [hp_X]/mL CALCIUM IODIDE;
  • 30 [hp_X]/mL CALCIUM OXALATE MONOHYDRATE;
  • 20 [hp_X]/mL ELAEIS GUINEENSIS FRUIT;
  • 22 [hp_X]/mL HELIANTHUS ANNUUS FLOWERING TOP;
  • 14 [hp_X]/mL HYDRANGEA ARBORESCENS ROOT;
  • 24 [hp_X]/mL IPECAC;
  • 23 [hp_X]/mL IRIS GERMANICA VAR. FLORENTINA ROOT;
  • 22 [hp_X]/mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE;
  • 22 [hp_X]/mL MANGANESE ACETATE TETRAHYDRATE;
  • 30 [hp_X]/mL MERCURIUS SOLUBILIS;
  • 22 [hp_X]/mL OSMIUM;
  • 36 [hp_X]/mL PHOSPHORIC ACID;
  • 20 [hp_X]/mL POTASSIUM ARSENITE ANHYDROUS;
  • 30 [hp_X]/mL POTASSIUM CHLORATE;
  • 17 [hp_X]/mL SANGUINARINE NITRATE;
  • 27 [hp_X]/mL TELLURIUM;
  • 30 [hp_X]/mL ZINC GLUCONATE


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Bismuth [CS];
  • Bismuth [EPC];
  • Blood Coagulation Factor [EPC];
  • Blood Coagulation Factor [EPC];
  • Calcium [CS];
  • Calcium [CS];
  • Calculi Dissolution Agent [EPC];
  • Cations;
  • Divalent [CS];
  • Cations;
  • Divalent [CS];
  • Cell-mediated Immunity [PE];
  • Copper Absorption Inhibitor [EPC];
  • Decreased Copper Ion Absorption [PE];
  • Increased Coagulation Factor Activity [PE];
  • Increased Coagulation Factor Activity [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [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];
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE];
  • Magnesium Ion Exchange Activity [MoA];
  • Magnetic Resonance Contrast Activity [MoA];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Osmotic Activity [MoA];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Osmotic Laxative [EPC];
  • Paramagnetic Contrast Agent [EPC];
  • Plant Proteins [CS];
  • Potassium Compounds [CS];
  • Potassium Salt [EPC];
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Labeler Information

Labeler Name: Vitality Works, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/20/2013

Package Information

No. Package Code Package Description Billing Unit
164616-109-0259 mL in 1 BOTTLE, DROPPER (64616-109-02)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64616-109The 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 NAMECal-5-ReviveThe 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 BalanceThe 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 DATE3/20/2013This 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 NAMEVitality Works, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACONITUM NAPELLUS; BISMUTH SUBNITRATE; CALCIUM ARSENATE; CALCIUM FLUORIDE; CALCIUM HYDROXIDE; CALCIUM IODIDE; CALCIUM OXALATE MONOHYDRATE; ELAEIS GUINEENSIS FRUIT; HELIANTHUS ANNUUS FLOWERING TOP; HYDRANGEA ARBORESCENS ROOT; IPECAC; IRIS GERMANICA VAR. FLORENTINA ROOT; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MANGANESE ACETATE TETRAHYDRATE; MERCURIUS SOLUBILIS; OSMIUM; PHOSPHORIC ACID; POTASSIUM ARSENITE ANHYDROUS; POTASSIUM CHLORATE; SANGUINARINE NITRATE; TELLURIUM; ZINC GLUCONATEAn 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 STRENGTH20; 15; 12; 25; 27; 10; 30; 20; 22; 14; 24; 23; 22; 22; 30; 22; 36; 20; 30; 17; 27; 30 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Bismuth [CS], Bismuth [EPC], Blood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Calcium [CS], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased IgG Production [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], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Magnetic Resonance Contrast Activity [MoA], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC], Plant Proteins [CS], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] 

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This page was last updated on: 2/1/2023