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Name:Alpha Cf
Manufacturer:Nature's Way Products, Inc.
Category:Homeopathic Marketed Drugs


Alpha CF

ALPHA CF  - aconitum napellus, bryonia alba root, eucalyptus globulus leaf, eupatorium perfoliatum flowering top, gelsemium sempervirens root, ipecac and phosphorus tablet 
Nature's Way Products, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Alpha CF

ACTIVE INGREDIENTS HPUS:

Aconitum napellus 4X

Bryonia alba 4X

Eucalyptus globulus 2X

Eupatorium perfoliatum 2X

Gelsemium sempervirens 4X

Ipecacuanha 3X

Phosphorus 6X

INACTIVE INGREDIENT:

Lactose

PURPOSE:

Temporarily relieves fever, chills, sneezing, stuffed-up nose, runny nose, coughing, sore throat, headache, minor aches and pains that may accompany colds or flu.

Keep out of the reach of children


INDICATIONS AND USAGE:

Temporarily relieves fever, chills, sneezing, stuffed-up nose, runny nose, coughing, sore throat, headache, minor aches and pains that may accompany colds or flu.

Directions:

Sublingual medication. Place tablets under tongue at least 15 minutes before or half hour after eating, brushing teeth, or drinking anything except water.

WARNINGS:

Consult a doctor if symptoms worsen, do not improve within 7 days, or new symptoms appear.  If fever lasts more than 3 days, or if sore throat is severe, persists for more than 2 days, or is accompanied or followed by fever, difficulty breathing, headache, rash, swelling, nausea, or vomiting, consult a doctor.  If cough persists for more than 7 days, tends to recur, or is accompanied by a rash or persistent headache, consult a doctor.  A persistent cough may be a sign of a serious condition.  Do not take this product for persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema or if cough is accompanied by excessive phlegm (mucus) unless directed by a doctor.  As with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using this product. 

DOSAGE:

Adults and children 12 years of age and older:  At first sign of cold or flu, take 1 tablet every hour and 2 or 3 tablets before gong to sleep.  As symptoms subside, take 1 tablet every 2 or 3 hours.

Children 2 to 12:  Half of the adult dose.

Children under 2:  Consult a doctor

Alpha CF 21803398 Carton

Alpha CF 21803398 Carton




ALPHA CF 
aconitum napellus, bryonia alba root, eucalyptus globulus leaf, eupatorium perfoliatum flowering top, gelsemium sempervirens root,ipecac tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:53499-0490
Route of Administration SUBLINGUAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACONITUM NAPELLUS (ACONITUM NAPELLUS) ACONITUM NAPELLUS 4 [hp_X]
BRYONIA ALBA ROOT (BRYONIA ALBA ROOT) BRYONIA ALBA ROOT 4 [hp_X]
EUCALYPTUS GLOBULUS LEAF (EUCALYPTUS GLOBULUS LEAF) EUCALYPTUS GLOBULUS LEAF 2 [hp_X]
EUPATORIUM PERFOLIATUM FLOWERING TOP (EUPATORIUM PERFOLIATUM FLOWERING TOP) EUPATORIUM PERFOLIATUM FLOWERING TOP 2 [hp_X]
GELSEMIUM SEMPERVIRENS ROOT (GELSEMIUM SEMPERVIRENS ROOT) GELSEMIUM SEMPERVIRENS ROOT 4 [hp_X]
IPECAC (IPECAC) IPECAC 3 [hp_X]
PHOSPHORUS (PHOSPHORUS) PHOSPHORUS 6 [hp_X]
Inactive Ingredients
Ingredient Name Strength
LACTOSE  
CELLULOSE, MICROCRYSTALLINE  
MAGNESIUM STEARATE  
Product Characteristics
Color white (B;T) Score no score
Shape ROUND (BT) Size 8mm
Flavor Imprint Code B;T
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53499-0490-1 4 BLISTER PACK ( BLISTER PACK) in 1 BOX contains a BLISTER PACK
1 10 TABLET ( TABLET) in 1 BLISTER PACK This package is contained within the BOX (53499-0490-1)
2 NDC:53499-0490-2 1 BOTTLE, GLASS ( BOTTLE) in 1 BOX contains a BOTTLE, GLASS
2 120 TABLET ( TABLET) in 1 BOTTLE, GLASS This package is contained within the BOX (53499-0490-2)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 07/01/2004

Labeler - Nature's Way Products, Inc. (153970520)
Establishment
Name Address ID/FEI Operations
V.S.M. Geneesmiddelen B.V. 407410919 manufacture

Revised: 05/2011 Nature's Way Products, Inc.



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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