EndoPure Pro description, usages, side effects, indications, overdosage, supplying and lots more!

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EndoPure Pro

The Wellness Center
Apotheca Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS

L-Arginine 6X, Pineal (Suis) 6X, Pituitary (Suis) 6X, Progesteroninum 6X, Belladonna 6C, Chelidonium Majus 6C, Dioscorea Villosa 6C, Folliculinum 6C, Glandula Suprarenalis Suis 6C, Hypothalamus (Suis) 6C, Oophorinum (Suis) 6C, Lilium Tigrinum 12C, Pulsatilla 12C, Sepia 12C, Sulphur 12C

INDICATIONS

For the temporary relief of hot flashes, stopped, scanty or late menses, liver and sleep complaints, vaginal and uterine irritability.

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 around neck is broken or missing. Store in a cool, dry place.

DIRECTIONS

5 drops orally 2 to 3 times daily between meals. Use Day 10 through 21 of the normal menstral cycle, even if menses has ceased. If cycle dates are unknown, day 1 is the first day of the calender month. Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS

Demineralized Water, 25% Ethanol

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS AND USAGE

For the temporary relief of hot flashes, stopped, scanty or late menses, liver and sleep complaints, vaginal and uterine irritability.

QUESTIONS

Manufactured for

The Wellness Center for Research and Eduction, Inc.

1237 S. Victoria Ave., Ste. 169

Oxnard, CA 93035

www.wellnesscenter.net

NDC 50181-0022-1

EndoPure

by Theresa Dale, Ph.D, CCN

Homeopathic

PRO

HORMONE REJUVENATION SYSTEM

1 FL. OZ. (30 ml)

EndoPure Pro

EndoPure Pro

L Arginine, Pineal, Pituitary, Progesteronium, Belladonna, Chelidonium Majus, Dioscorea Villosa, Folliculinum LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50181-0022
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ARGININE 6 [hp_X]
SUS SCROFA PINEAL GLAND SUS SCROFA PINEAL GLAND 6 [hp_X]
SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND 6 [hp_X]
progesterone PROGESTERONE 6 [hp_X]
ATROPA BELLADONNA WHOLE ATROPA BELLADONNA WHOLE 6 [hp_C]
CHELIDONIUM MAJUS CHELIDONIUM MAJUS 6 [hp_C]
DIOSCOREA VILLOSA TUBER DIOSCOREA VILLOSA TUBER 6 [hp_C]
ESTRONE ESTRONE 6 [hp_C]
SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND 6 [hp_C]
SUS SCROFA HYPOTHALAMUS SUS SCROFA HYPOTHALAMUS 6 [hp_C]
SUS SCROFA OVARY SUS SCROFA OVARY 6 [hp_C]
LILIUM LANCIFOLIUM WHOLE FLOWERING LILIUM LANCIFOLIUM WHOLE FLOWERING 12 [hp_C]
PULSATILLA VULGARIS PULSATILLA VULGARIS 12 [hp_C]
SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE 12 [hp_C]
SULFUR SULFUR 12 [hp_C]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50181-0022-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-01-08


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