NDC 62795-1042 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 And Influenza A Virus A/singapore/6/86 (h1n1) Antigen (heat Inactivated)

NDC Product Code 62795-1042

NDC 62795-1042-2

Package Description: 1 BOTTLE in 1 CARTON > 60 TABLET in 1 BOTTLE

NDC Product Information

Reboost with NDC 62795-1042 is a a human over the counter drug product labeled by Medinatura Inc.. The generic name of Reboost is 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 and influenza a virus a/singapore/6/86 (h1n1) antigen (heat inactivated). The product's dosage form is tablet and is administered via oral form.

Labeler Name: Medinatura Inc.

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

Product Type: Human Otc Drug 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.

Reboost Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ACONITUM NAPELLUS 3 [hp_X]/1
  • BRYONIA ALBA ROOT 3 [hp_X]/1
  • EUPATORIUM PERFOLIATUM FLOWERING TOP 6 [hp_X]/1
  • LACHESIS MUTA VENOM 10 [hp_X]/1
  • GOLDENSEAL 5 [hp_X]/1
  • PHOSPHORUS 8 [hp_X]/1
  • VINCETOXICUM HIRUNDINARIA ROOT 6 [hp_X]/1
  • ZINC GLUCONATE 1 [hp_X]/1
  • ZINC ACETATE ANHYDROUS 2 [hp_X]/1
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 20 [hp_X]/1
  • IPECAC 3 [hp_X]/1
  • SULFUR 4 [hp_X]/1
  • INFLUENZA A VIRUS A/SINGAPORE/6/86 (H1N1) ANTIGEN (HEAT INACTIVATED) 19 [hp_X]/1

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
  • LEMON (UNII: 24RS0A988O)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Medinatura Inc.
Labeler Code: 62795
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 02-19-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Reboost Product Label Images

Reboost Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Uses

Uses: To reduce minor cold and flu symptoms: Chills,Cough, Headache, Body aches, Fatigue, Runny nose,Chest congestion and Nausea

Warnings

Warnings: If pregnant or breast-feeding, ask ahealth professional before use. Keep out of reach ofchildren. If symptoms persist or worsen, a healthprofessional should be consulted. Do not use if knownsensitivity to ReBoostTM or any of its ingredients exists

Directions

Directions: For max absorption, dissolve undertongue. Can be chewed and swallowed. Adults andchildren 12 years and older: 2 tablets every 4 hours.Do not exceed 12 tablets per 24 hours. Children 4 to11 years: 1-2 tablets every 4 hours. Do not exceed12 tablets per 24 hours. For children under 4 years,consult your health professional.

Active Ingredients

Zincum aceticum 2X 50mgZincum gluconicum 1X 50mg*Asclepias vincetoxicum 6X, 10X, 30X 20mg each*Anas barbariae 20X, 200C 20mg each*Aconitum napellus 3X 20mg*Bryonia 3X 20mg*Ipecacuanha 3X 20mg*Sulphur 4X, 10X 20 mg each*Hydrastis canadensis 5X 20mg*Eupatorium perfoliatum 6X 20mg.Phosphorus 8X 20mg*Lachesis mutus 10X 20mg*Influenzinum 19X 20mg*Natural Ingredient

Inactive Ingredients

Citric acid, Lactose, OrganicLemon flavor with other natural flavors, Magnesiumstearate, Organic Stevia

Purpose

Reduces cold and flu symptomsRelieves chills, headaches, bodyachesRelieves fatigueRelieves nauseaRelieves chest congestionRelieves cough, runny nose

* Please review the disclaimer below.