SMART HCG- human chorionic gonadortopin, liquid

Smart HCG by

Drug Labeling and Warnings

Smart HCG by is a Homeopathic medication manufactured, distributed, or labeled by Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS:  Human chorionic gonadotropin (hcg) 8X, 12X, 30X, 60X.

PURPOSE

INDICATIONS:  Detox, appetite control, supports normal fat loss and normal muscle building when used in conjunction with the HCG program.

WARNINGS

WARNINGS:  If pregnant or breast-feeding, do not 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.

DOSAGE & ADMINISTRATION

DIRECTIONS:  Adults: 1/2 dropper twice daily.  Place drops under tongue.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:  Demineralized water, 20% Ethanol.

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.

INDICATIONS & USAGE

INDICATIONS:  Detox, appetite control, supports normal fat loss and normal muscle building when used in conjunction with the HCG program.

QUESTIONS

Distributed By:

Smart HCG

World Trade Center 180-A22

2050 Stemmons Freeway

Dallas, TX 75207-3101

PRINCIPAL DISPLAY PANEL

NDC: 57520-0337-1

HOMEOPATHIC MEDICINE

Smart HCG

HOMEOPATHIC HCG

1 fl. oz. (30 ml)

INGREDIENTS AND APPEARANCE

SMART HCG 
human chorionic gonadortopin, liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57520-0337
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HUMAN CHORIONIC GONADOTROPIN (UNII: 20ED16GHEB) (HUMAN CHORIONIC GONADOTROPIN - UNII:20ED16GHEB)	HUMAN CHORIONIC GONADOTROPIN	60 [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: 57520-0337-1	30 mL in 1 BOTTLE, DROPPER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		11/10/2010

Labeler - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture