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

Coniferyl Alcohol

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
Coniferyl Alcohol



FULL PRESCRIBING INFORMATION

Active ingredient

ACTIVE INGREDIENTS:  Coniferyl alcohol 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.


Purpose

INDICATIONS:  For temporary relief of symptoms caused by allergies including rhinitis, congestion, headaches, digestive problems and rashes.


WARNINGS:  Keep out of reach of children.  In case of overdose, contact physician or Poison Control Center right away.

If pregnant or breast-feeding, seek advice of a health professional before use.

Tamper seal:  "Sealed for Your Protection."  Do not use if seal is broken or missing.


DIRECTIONS:  1-10 drops under the tongue, 3 times a day or as directed by a health professional.  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, contact physician or Poison Control Center right away.


Uses

INDICATIONS:  For temporary relief of symptoms caused by allergies including rhinitis, congestion, headaches, digestive problems and rashes.


Dist. By:

Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com


DESBIO

NDC 57520-0797-1

HOMEOPATHIC

CONIFERYL ALCOHOL

1 FL OZ (30 ml)

Coniferyl Alcohol

Coniferyl alcohol, LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57520-0797
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CONIFERYL ALCOHOL Coniferyl Alcohol 6 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57520-0797-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-08-24


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