Reboost description, usages, side effects, indications, overdosage, supplying and lots more!

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Reboost

Heel Inc.

Reboost Tablet


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS

Active Ingredients: Each tablet contains: Aconitum napellus 4X, Bryonia alba 4X, Eupatorium perfollatum 3X, Lachesis mutus 12X, Phosphorus 5X

INACTIVE INGREDIENTS

Inactive Ingredients: Lactose and Magnessium stearate

PURPOSE

Aconitum napellus 4X................Relieves headache

Bryonia alba 4X.........................Relieves body aches

Eupatorium perfollatum 3X.......Relieves headache and body aches

Lachesis mutus 12X..................Relieves cough

Phosphorus 5X..........................Relieves fatigue

REBOOST DOSAGE AND ADMINISTRATION

Standard Dosage: Adults and children 12 years and older: 3 tablets per day, taking 1 tablet every 4 to 6 hours.

Children 4 to 11 years: 2 tablets per day, taking 1 tablet every 6 to 8 hours.

For children under 4 years, consult your healthcare provider.

Initial Dosage: Adults and children 12 years and older: 1 tablet every 1/2 to 1 hour, until symptoms lessen, then continue with standard dosage. Do not exceed 12 tablets in 24 hours.

Children 4 to 11 years: 1 tablet every 1/2 to 1 hour, until symptoms lessen, then continue with standard dosage. Do not exceed 8 tablets in 24 hours.

For children under 4 years, consult your healthcare provider.

Allow tablets to dissolve completely in mouth, do not swallow.

WARNINGS

In isolated cases allergic skin reactions may occur. If pregnant or breast-feeding, ask a healthcare provider before use. Keep out of reach of children. If symptoms persist or worsen, a healthcare provider should be consulted. Do not use if known sensitivity to Reboost or any of its ingredients exists.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

REBOOST INDICATIONS AND USAGE

For the temporary relief of minor flu symptoms:

  • Body aches
  • Fatigue
  • Headache

Reboost

Reboost

ACONITUM NAPELLUS and BRYONIA ALBA ROOT and EUPATORIUM PERFOLIATUM FLOWERING TOP and LACHESIS MUTA VENOM and PHOSPHORUS TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50114-8105
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ACONITUM NAPELLUS ACONITUM NAPELLUS 4 [hp_X]
BRYONIA ALBA ROOT BRYONIA ALBA ROOT 4 [hp_X]
EUPATORIUM PERFOLIATUM FLOWERING TOP EUPATORIUM PERFOLIATUM FLOWERING TOP 3 [hp_X]
LACHESIS MUTA VENOM LACHESIS MUTA VENOM 12 [hp_X]
PHOSPHORUS PHOSPHORUS 5 [hp_X]

Inactive Ingredients

Ingredient Name Strength
LACTOSE
MAGNESIUM STEARATE

Product Characteristics

Color Size Imprint Code Shape
white 9 mm Heel ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 100 in 1 BOTTLE
2 NDC:50114-8105-2 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-01-28


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Be sure to consult your doctor before taking any medication!
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