GUNA-BDNF description, usages, side effects, indications, overdosage, supplying and lots more!

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GUNA-BDNF

Guna spa

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

BRAIN-DERIVED NEUROTROPHIC FACTOR     4C

PURPOSE

Neurotrophic Support

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of reach of children

INDICATIONS & USAGE

Neurotrophic Support

WARNINGS

Stop use and ask doctor if symptoms worsen or persist more than 3 days

DIRECTIONS

Take 15 minutes before meals.
Adults and children 12 years and older    20 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow.
Children  between 12 years and 6 years of age    10 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow.
Children under 6 years     5 drops twice a day in a glass of water.

INACTIVE INGREDIENT

Ethyl Alcohol 30%

PRINCIPAL DISPLAY PANEL

GUNA-BDNF

GUNA-BDNF

BRAIN-DERIVED NEUROTROPHIC FACTOR SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:17089-370
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BRAIN-DERIVED NEUROTROPHIC FACTOR HUMAN BRAIN-DERIVED NEUROTROPHIC FACTOR HUMAN 4 [hp_C]

Inactive Ingredients

Ingredient Name Strength
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 30 in 1 BOTTLE, DROPPER
2 NDC:17089-370-18 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-03-31


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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