Influenza Remedy description, usages, side effects, indications, overdosage, supplying and lots more!

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Influenza Remedy

Deseret Biologicals
Apotheca Company

DRUG FACTS:


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS:

Eucalyptus Globulus 2X, 10X, 30X, Ipecacuanha 3X, 10X, 30X, Aconitum Napellus 3X, 10X, 30X, 200X

INDICATIONS:

For temporary relief of symptoms related to influenza infection including high fever, headache, fatigue, cough, irritated throat, runny and/or stuffy nose, body aches, vomiting and diarrhea.

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.

KEEP OUT OF REACH OF CHILDREN:

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

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.

INDICATIONS:

For temporary relief of symptoms related to influenza infection including high fever, headache, fatigue, cough, irritated throat, runny and/or stuffy nose, body aches, vomiting and diarrhea.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070  www.desbio.com

PACKAGE DISPLAY LABEL:

DESBIO

NDC 43742-0238-1

​INFLUENZA REMEDY

​1 FL OZ (30 ml)

Influenza Remedy

Influenza Remedy

Eucalyptus Globulus, Ipecacuanha, Aconitum Napellus LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43742-0238
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
EUCALYPTUS GLOBULUS LEAF EUCALYPTUS GLOBULUS LEAF 2 [hp_X]
Ipecac IPECAC 3 [hp_X]
ACONITUM NAPELLUS ACONITUM NAPELLUS 3 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43742-0238-1 30 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-10-16


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