62795-1044 NDC - REBOOST (ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GOLDENSEAL, LACHESIS MUTA VENOM, PHOSPHORUS, VINCETOXICUM HIRUNDINARIA ROOT, ZINC GLUCONATE, ZINC ACETATE ANHYDROUS, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, IPECAC, SULFUR)

Drug Information

  • Product NDC: 62795-1044
  • Proprietary Name: Reboost
  • Non Proprietary Name: ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GOLDENSEAL, LACHESIS MUTA VENOM, PHOSPHORUS, VINCETOXICUM HIRUNDINARIA ROOT, ZINC GLUCONATE, ZINC ACETATE ANHYDROUS, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, IPECAC, SULFUR
  • Active Ingredient(s): 3 [hp_X]/1 ACONITUM NAPELLUS; 3 [hp_X]/1 BRYONIA ALBA ROOT; 20 [hp_X]/1 CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE; 6 [hp_X]/1 EUPATORIUM PERFOLIATUM FLOWERING TOP; 5 [hp_X]/1 GOLDENSEAL; 3 [hp_X]/1 IPECAC; 10 [hp_X]/1 LACHESIS MUTA VENOM; 8 [hp_X]/1 PHOSPHORUS; 4 [hp_X]/1 SULFUR; 6 [hp_X]/1 VINCETOXICUM HIRUNDINARIA ROOT; 2 [hp_X]/1 ZINC ACETATE ANHYDROUS; 1 [hp_X]/1 ZINC GLUCONATE
  • Administration Route(s): ORAL
  • Dosage Form(s): TABLET
  • Pharmacy Class(es): Copper Absorption Inhibitor [EPC]; Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]; Decreased Copper Ion Absorption [PE]

Labeler Information

Field Name Field Value
Labeler Name: MediNatura Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:1/5/2022

Package Information

No. Package Code Package Description Billing Unit
162795-1044-21 BOTTLE in 1 CARTON (62795-1044-2) / 60 TABLET in 1 BOTTLEEA

NDC Record

Field Name Field Value Definition
PRODUCT NDC62795-1044The 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 NAMEReboostThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GOLDENSEAL, LACHESIS MUTA VENOM, PHOSPHORUS, VINCETOXICUM HIRUNDINARIA ROOT, ZINC GLUCONATE, ZINC ACETATE ANHYDROUS, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, IPECAC, SULFURThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLETThe 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 DATE1/5/2022This 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 NAMEMediNatura Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACONITUM NAPELLUS; BRYONIA ALBA ROOT; CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE; EUPATORIUM PERFOLIATUM FLOWERING TOP; GOLDENSEAL; IPECAC; LACHESIS MUTA VENOM; PHOSPHORUS; SULFUR; VINCETOXICUM HIRUNDINARIA ROOT; ZINC ACETATE ANHYDROUS; 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 STRENGTH3; 3; 20; 6; 5; 3; 10; 8; 4; 6; 2; 1 
ACTIVE INGRED UNIT[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 
PHARM CLASSESCopper Absorption Inhibitor [EPC], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Decreased Copper Ion Absorption [PE] 

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This page was last updated on: 11/21/2025

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