FDA.reportPublic FDA data

ReBoost Flu Symptom Berry Tablet

Manufacturer
MediNatura
Effective date
2017-12-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:05:11

Label at a glance#

ProductReBoost Flu Symptom Relief Berry
Active ingredientACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GOLDENSEAL, LACHESIS MUTA VENOM, PHOSPHORUS
Label structure8 sections

Indications and uses

Uses :  For the temporary relief of minor cold and flu symptoms: • Congestion • Runny Nose • Body Aches

Dosage and administration

Directions: Adults and children 12 years and older: Chew 2-3 tablets every 4 hours. Do not exceed 18 tablets per 24 hours. Children 4 to 11 years: Chew 1-2 tablets every 4 hours. Do not exceed 12 tablets per 24 hours. For children under 4 years, consult your health professional. Allow tablets to dissolve completely in the mouth

Label contents#

Full prescribing information#

PURPOSE

OTC - PURPOSE SECTION

Relieves

• Congestion

• Runny Nose

• Body Aches

USES

INDICATIONS & USAGE SECTION

Uses :

 For the temporary relief of minor cold and flu symptoms:

• Congestion

• Runny Nose

• Body Aches

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Directions:

Adults and children 12 years and older:

Chew 2-3 tablets every 4 hours. Do not exceed 18 tablets per 24 hours.

Children 4 to 11 years:

Chew 1-2 tablets every 4 hours. Do not exceed 12 tablets per 24 hours.

For children under 4 years, consult your health professional.

Allow tablets to dissolve completely in the mouth

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Each tablet contains

Active Ingredients

*Aconitum napellus 4X 120mg, *Bryonia alba 3X 7mg, *Eupatorium perfoliatum 3X 30mg *Hydrastis canadensis 6X 53mg,*Lachesis mutus 10X 60mg,  Phosphorus 8X 30mg

*Natural Ingredients

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Citric acid, Lactose, Magnesium stearate, Organic Berry flavor blend with other natural flavors (4.5%),Organic Stevia (0.1%)

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

WARNINGS

WARNINGS SECTION

Warnings:

In isolated cases allergic skin reactions may occur. 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 ReBoost™ or any of its ingredients exists.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ReBoost Flu Symptom Berry Tablet.jpgReBoost Flu Symptom Berry Tablet.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62795-1037-22020-02-11C16284748780-19d75b9cf-daa5-f424-e053-dadaa90a57ceReBoost Flu Symptom Berry Tablet
62795-1037-22020-01-31C16284748780-19d75b9cf-daa5-f424-e053-dadaa90a57ceReBoost Flu Symptom Berry Tablet

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62795-1037-2EA - Each62795-1037be4173f7-dabe-49cf-8ca2-645f1d912e5d12016-11-08

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62795-103762795-1037-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACONITUM NAPELLUSU0NQ8555JDACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
EUPATORIUM PERFOLIATUM FLOWERING TOP1W0775VX6EACTIB
GOLDENSEALZW3Z11D0JVACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
PHOSPHORUS27YLU75U4WACTIB
LACTOSEJ2B2A4N98GIACT
MAGNESIUM STEARATE70097M6I30IACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
STEVIA REBAUDIUNA LEAF6TC6NN0876IACT

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
3b9fa542-0ffc-467d-a6f9-05ce1e418003268ac416-71e7-4b6c-960e-913672acce9b2017-12-20WarningsExact identifier
spl id: 3b9fa542-0ffc-467d-a6f9-05ce1e418003
spl set id: 268ac416-71e7-4b6c-960e-913672acce9b

Reported adverse events (FAERS/openFDA)#

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