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Allerstat

Energique, Inc.
Apotheca Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS:

Baptisia tinctoria 3X, Echinacea (angustifolia) 3X, Allium cepa 12X, Ambrosia artemsiaefolia 12X, Arsenicum album 12X, Euphrasia officinalis 12X, Natrum sulphuricum 12X, Nux vomica 12X, Phosphorus 12X, Pulsatilla (vulgaris) 12X, Solidago virgaurea 12X, Sulphur 12X.

INDICATIONS:

For temporary relief of sinus congestion due to hay fever and allergic rhinitis.**

**These statements are based upon traditional homeopathic practice.  They have not been review by the Food and Drug Administration.

WARNINGS:

If pregnant or breast-feeding, ask a health 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 a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

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

DIRECTIONS:

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional.  If symptoms persist, consult your health care professional. 

Consult a physician for use in children under 12 years of age.

INDICATIONS:

For temporary relief of sinus congestion due to hay fever and allergic rhinitis.**

**These statements are based upon traditional homeopathic practice. The have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

Demineralized water, 20% Ethanol.

QUESTIONS:

Dist. by Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579

800-869-8078

PACKAGE LABEL DISPLAY

ENERGIQUE

since 1987

HOMEOPATHIC REMEDY

ALLERSTAT II

2 fl. oz. (60 ml)

Allerstat

Allerstat

Baptisia tinctoria, Echinacea (angustifolia), Allium cepa, Ambrosia artemisiaefolia, Arsenicum album, Euphrasia officinalis, Natrum sulphuricum, LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:44911-0111
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BAPTISIA TINCTORIA ROOT BAPTISIA TINCTORIA ROOT 3 [hp_X]
ECHINACEA ANGUSTIFOLIA ECHINACEA ANGUSTIFOLIA 3 [hp_X]
ONION ONION 12 [hp_X]
AMBROSIA ARTEMISIIFOLIA AMBROSIA ARTEMISIIFOLIA 12 [hp_X]
ARSENIC TRIOXIDE ARSENIC TRIOXIDE 12 [hp_X]
EUPHRASIA STRICTA EUPHRASIA STRICTA 12 [hp_X]
SODIUM SULFATE SODIUM CATION 12 [hp_X]
STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED 12 [hp_X]
PHOSPHORUS PHOSPHORUS 12 [hp_X]
PULSATILLA VULGARIS PULSATILLA VULGARIS 12 [hp_X]
SOLIDAGO VIRGAUREA FLOWERING TOP SOLIDAGO VIRGAUREA FLOWERING TOP 12 [hp_X]
SULFUR SULFUR 12 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:44911-0111-1 60 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2014-03-17


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