Psorinum by Energique, Inc. / Apotheca Company PSORINUM liquid

Psorinum by

Drug Labeling and Warnings

Psorinum by is a Homeopathic medication manufactured, distributed, or labeled by Energique, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT:

PSORINUM 7X

INDICATIONS:

To be used according to standard homeopathic indications.**

**These statements are based upon traditional homeopathic practice.  They have not been reviewed 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.

RX ONLY:

Caution: Federal law prohibits dispensing without prescription.

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, 1 time daily or as otherwise directed.  If symptoms persist, consult your health care professional.  Consult a physician for use in children under 12 years of age.

INDICATIONS:

To be used according to standard homeopathic indications.**

**These statements are based upon traditional homeopathic practice. They 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

PSORINUM 7X

1fl. oz. (30 ml)

RX ONLY:

Caution: Federal law prohibits dispensing without prescription.

INGREDIENTS AND APPEARANCE

PSORINUM 
psorinum liquid

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 44911-0097
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4) (SCABIES LESION LYSATE (HUMAN) - UNII:5UAU16Z1U4)	SCABIES LESION LYSATE (HUMAN)	7 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44911-0097-1	30 mL in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		12/09/2014

Labeler - Energique, Inc. (789886132)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(44911-0097) , api manufacture(44911-0097) , label(44911-0097) , pack(44911-0097)