EndoPure Pro

Manufacturer
The Wellness Center for Research and Education, Inc. | Apotheca Company
Effective date
2025-06-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:37:09

Label at a glance#

ProductEndoPure Pro
Active ingredientARGININE, SUS SCROFA PITUITARY GLAND, SUS SCROFA PINEAL GLAND, PROGESTERONE, ATROPA BELLADONNA, CHELIDONIUM MAJUS, DIOSCOREA VILLOSA TUBER, ESTRONE, SUS SCROFA ADRENAL GLAND, SUS SCROFA HYPOTHALAMUS, SUS SCROFA OVARY, LILIUM LANCIFOLIUM WHOLE FLOWERING, PULSATILLA VULGARIS WHOLE, SEPIA OFFICINALIS JUICE, SULFUR
Label structure9 sections

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

L-Arginine 6X, Hypophysis Suis 6X, Pineal (Suis) 6X, Progesterone 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 (Vulgaris) 12C, Sepia 12C, Sulphur 12C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

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

WARNINGS:

WARNINGS SECTION

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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Manufactured for

The Wellness Center for Research

and Education, Inc.

1237 S. Victoria Ave., Suite 169

Oxnard, CA 93035

www.wellnesscenter.net

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 50181-0066-1

EndoPure

by Theresa Dale, Ph.D, CCN

Homeopathic

PRO

HORMONE REJUVENATION SYSTEM

1 FL. OZ. (30 ml)

EndoPure ProEndoPure Pro

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50181-0066-12025-06-06C16284748780-1ba0f9c33-261d-a910-e053-dadaa90a0b85Drug Facts:
50181-0066-12021-01-29C16284748780-1ba0f9c33-261d-a910-e053-dadaa90a0b85Drug Facts:

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50181-006650181-0066-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
bd49cc55-7777-49c5-a9d6-ffa1270f448f63edf9f0-60a1-4e2b-83df-3e69490f1ef72025-06-06WarningsExact identifier
spl id: bd49cc55-7777-49c5-a9d6-ffa1270f448f
spl set id: 63edf9f0-60a1-4e2b-83df-3e69490f1ef7

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.