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

Bio Electrolyte

BioActive Nutritional, Inc.
Apotheca Company

  • 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
Drug Facts

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS

Boricum Gluconicum 6X, Calcarea Gluconica 6X, Chromium Gluconicum 6X, Cobaltum Gluconicum 6X, Cuprum Gluconicum 6X, Ferrum Gluconicum 6X, Kali Gluconicum 6X, Magnesia Gluconica 6X, Manganum Gluconicum 6X, Natrum Gluconicum 6X, Niccolum Gluconicum 6X, Selenium Dioxide 6X, Zincum Gluconicum 6X, Kali Phosphoricum 8X, Vanadium Metallicum 8X, Calcarea Phosphorica 9X

INDICATIONS

To speed recovery time after extreme exertion.

WARNINGS

If pregnant or breast-feeding, ask a health care professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

Store in cool, dry place.

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS

Demineralized water, 25% Ethanol.

KEEP OUT OF REACH OF CHILDREN

In case of overdose, get medical help or contact a Poison Control Center right away.

INDICATIONS AND USAGE

To speed recovery time after extreme exertion.

QUESTIONS

Distributed by:

BIOACTIVE NUTRITIONAL

Melbourne, FL 32935

For Nutritional Information write:

BioActive Nutritional, Inc.

1803 N. Wickham Rd.

Melbourne, FL 32935

BioActive Homeopathic

BIO ELECTROLYTE

2 FL OZ (60 ml)

Bio Electrolyte

Boricum Gluconicum, Calcarea Gluconica, Chromium Gluconicum, Cobaltum Gluconicum, Cuprum Gluconicum LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43857-0121
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BORON GLUCONATE BORON 6 [hp_X]
Calcium Gluconate 6 [hp_X]
CHROMIUM GLUCONATE CHROMIUM 6 [hp_X]
COBALTOUS GLUCONATE COBALT 6 [hp_X]
COPPER GLUCONATE 6 [hp_X]
FERROUS GLUCONATE FERROUS CATION 6 [hp_X]
MAGNESIUM GLUCONATE Magnesium cation 6 [hp_X]
MANGANESE GLUCONATE MANGANESE CATION (2+) 6 [hp_X]
Sodium Gluconate 6 [hp_X]
NICKEL GLUCONATE NICKEL CATION 6 [hp_X]
SELENIUM DIOXIDE SELENIUM DIOXIDE 6 [hp_X]
ZINC GLUCONATE zinc 6 [hp_X]
potassium phosphate, dibasic PHOSPHATE ION 8 [hp_X]
VANADIUM VANADIUM 8 [hp_X]
TRIBASIC CALCIUM PHOSPHATE CALCIUM CATION 9 [hp_X]

Inactive Ingredients

Ingredient Name Strength
ASCORBIC ACID
Dextrose monohydrate
ALCOHOL
ARGININE
CARNITINE
LEUCINE
ORNITHINE
VALINE
MAGNESIUM CHLORIDE
GRAPE
potassium chloride
SODIUM CHLORIDE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43857-0121-1 60 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-01-29


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