FDA.reportPublic FDA data

Reboost

Manufacturer
MediNatura Inc.
Effective date
2021-11-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:27:02

Label at a glance#

ProductReboost
Active ingredientACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, LACHESIS MUTA VENOM, GOLDENSEAL, PHOSPHORUS, VINCETOXICUM HIRUNDINARIA ROOT, ZINC GLUCONATE, ZINC ACETATE ANHYDROUS, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, IPECAC, SULFUR, INFLUENZA A VIRUS A/SINGAPORE/6/86 (H1N1) ANTIGEN (HEAT INACTIVATED)
Label structure8 sections

Indications and uses

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

Dosage and 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: 1-2 tablets every 4 hours. Do not exceed 12 tablets per 24 hours. For children under 4 years, consult your health professional.

Label contents#

Full prescribing information#

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

USES

INDICATIONS & USAGE SECTION

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

WARNINGS

WARNINGS SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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: 1-2 tablets every 4 hours. Do not exceed
12 tablets per 24 hours. For children under 4 years,
consult your health professional.

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Zincum aceticum 2X 50mg
Zincum 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

INACTIVE INGREDIENT SECTION

Citric acid, Lactose, Organic
Lemon flavor with other natural flavors, Magnesium
stearate, Organic Stevia

PURPOSE

OTC - PURPOSE SECTION


Reduces cold and flu symptoms
Relieves chills, headaches, bodyaches
Relieves fatigue
Relieves nausea
Relieves chest congestion
Relieves cough, runny nose



PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Reboost.jpgReboost.jpg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62795-104262795-1042-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACONITUM NAPELLUSU0NQ8555JDACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
EUPATORIUM PERFOLIATUM FLOWERING TOP1W0775VX6EACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
GOLDENSEALZW3Z11D0JVACTIB
PHOSPHORUS27YLU75U4WACTIB
VINCETOXICUM HIRUNDINARIA ROOT9R858U917WACTIB
ZINC GLUCONATEU6WSN5SQ1ZACTIB
ZINC ACETATE ANHYDROUSH2ZEY72PMEACTIM
CAIRINA MOSCHATA HEART/LIVER AUTOLYSATERN2HC612GYACTIB
IPECAC62I3C8233LACTIB
SULFUR70FD1KFU70ACTIB
INFLUENZA A VIRUS A/SINGAPORE/6/86 (H1N1) ANTIGEN (HEAT INACTIVATED)WC4E824FQ9ACTIB
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
MAGNESIUM STEARATE70097M6I30IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
STEVIA REBAUDIUNA LEAF6TC6NN0876IACT
LEMON24RS0A988OIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
da0a425e-b716-4f93-9903-c3db9058abaf37da8f7b-5a42-4f1b-b227-612d152e21f52021-11-11WarningsExact identifier
spl id: da0a425e-b716-4f93-9903-c3db9058abaf
spl set id: 37da8f7b-5a42-4f1b-b227-612d152e21f5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.