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Reboost

Heel Inc

Reboost Cough Syrup


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS

Active Ingredients: Each 5ml contains: Antimonium tartaricum 6X, Cuprum sulphuricum 6X, Drosera rotundifolia 4X, Ipecacuanha 4X, Rumex crispus 4X, Spongia tosta 8X

INACTIVE INGREDIENTS

Inactive Ingredients: Purified Water, Honey, Preserved water and Simple syrup

PURPOSE

Antimonium tartaricum 6X..............Relieves chest congestion

Cuprum sulphuricum 6X.................Relieves cough

Drosera rotundifolia 4X..................Relieves cough

Ipecacuanha 4X.............................Relieves cough

Rumex crispus 4X...........................Relieves cough

Spongia tosta 8X...........................Relieves cough

REBOOST DOSAGE AND ADMINISTRATION

Standard Dosage: Adults and children 12 years and older: 2 teaspoons every 4 to 6 hours.

Children 4 to 11 tears: 1 teaspoon every 3 to 4 hours.

Children 1 to 4 years, consult your healthcare provider.

Initial Dosage: Adults and children 12 years and older: 2 teaspoons every 1 to 2 hours until symptoms lessen, then continue with standard dosage. Do not exceed 36 teaspoons in 24 hours.

Children 4 to 11 tears: 1 teaspoon every 1 to 2 hours until symptoms lessen, then continue with standard dosage. Do not exceed 18 teaspoons in 24 hours.

Children 1 to 4 years, consult your healthcare provider.

WARNINGS

Do not use in infants younger than 1 year due to the presence of honey. 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:

  • Chest Congestion
  • Cough due to colds and flu

Reboost

Reboost

ANTIMONY POTASSIUM TARTRATE SYRUP

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50114-8550
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Antimony Potassium Tartrate ANTIMONY CATION (3+) 6 [hp_X]
CUPRIC SULFATE CUPRIC CATION 6 [hp_X]
DROSERA ROTUNDIFOLIA DROSERA ROTUNDIFOLIA 4 [hp_X]
Ipecac IPECAC 4 [hp_X]
RUMEX CRISPUS ROOT Rumex Crispus Root 4 [hp_X]
SPONGIA OFFICINALIS SKELETON, ROASTED SPONGIA OFFICINALIS SKELETON, ROASTED 8 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
HONEY
propylene glycol
METHYLPARABEN
PROPYLPARABEN
SUCROSE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 125 in 1 BOTTLE
2 NDC:50114-8550-1 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-02-13


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Be sure to consult your doctor before taking any medication!
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