Gripp-Heel description, usages, side effects, indications, overdosage, supplying and lots more!

Gripp-Heel

Heel Inc

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Gripp-Heel Tablet

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

INDICATIONS AND USAGE

For the temporary relief of minor flu symptoms:

  • Body aches
  • Fatigue
  • Headache


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 Gripp-Heel® or any of its ingredients exists.

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 the mouth, do not swallow.

ACTIVE INGREDIENT

Each tablet contains as active ingredients: Aconitum napellus 4X,  Bryonia alba 4X, Lachesis mutus 12X, Eupatorium perfoliatum 3X, Phosphorus 5X.

INACTIVE INGREDIENT

Lactose, Magnesium Stearate

PURPOSE

Body aches, Fatigue, Headache

Gripp-Heel

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

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50114-6075
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]
LACHESIS MUTA VENOM LACHESIS MUTA VENOM 12 [hp_X]
EUPATORIUM PERFOLIATUM FLOWERING TOP EUPATORIUM PERFOLIATUM FLOWERING TOP 3 [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 NDC:50114-6075-2 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
1984-01-31


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Be sure to consult your doctor before taking any medication!
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