Drugplain

Reboost 3 [hp_X]/1

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 · TABLET · MediNatura Inc.

1 Recall on Record
Plain English

Reboost is a tablet containing 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 at 3 [hp_X]/1, taken oral. Manufactured by MediNatura Inc..

Key Facts

Brand Name
Reboost
Generic 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
NDC Code (Product)
62795-1044
Manufacturer
MediNatura Inc.
Strength
3 [hp_X]/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Marketing Start
01/05/2022

Recall History

1 Recall on Record
Class I12/12/2025

Medinatura New Mexico, inc.

Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.

OngoingVoluntary: Firm initiated

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

abdominal discomfort1 reports
concussion1 reports
contusion1 reports
dizziness1 reports
dyspnoea1 reports
epistaxis1 reports
fall1 reports
fatigue1 reports
flushing1 reports
head injury1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

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

Dosage & Administration

Directions: For max absorption, dissolve under tongue. Can be chewed and swallowed. Adults and children 12 years and older: 2 tablets every 4 hours. Do not exceed 12 tablets per 24 hours. Children 4 to 11 years: 1 tablet every 4 hours. Do not exceed 6 tablets per 24 hours. For children under 4 years, consult your health professional.

Warnings

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

Frequently Asked Questions

What is Reboost used for?

Reboost contains 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. It is a tablet taken oral. Consult your doctor for specific uses.

Is Reboost a controlled substance?

Reboost is not classified as a controlled substance by the DEA.

What is the generic name for Reboost?

The generic name for 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. There are no other listed brand versions of 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.

What is the NDC code for Reboost 3 [hp_X]/1?

The NDC (National Drug Code) for Reboost 3 [hp_X]/1 is 62795-1044, listed by MediNatura Inc..

Product NDC

62795-1044

Package NDC

62795-1044-2

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)