EndoPure Estro

Manufacturer
The Wellness Center for Research and Education | Apotheca Company
Effective date
2025-06-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:37:10

Label at a glance#

ProductEndoPure Estro
Active ingredientESTRADIOL, ESTRIOL, ESTRONE, ATROPA BELLADONNA, CHELIDONIUM MAJUS, SUS SCROFA ADRENAL GLAND, HYDROCORTISONE, SUS SCROFA HYPOTHALAMUS, SUS SCROFA OVARY, SUS SCROFA PINEAL GLAND, SUS SCROFA PITUITARY GLAND, SANGUINARIA CANADENSIS ROOT, 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. Administer orally, day 1 through 24 of the monthly menstrual cycle, even if menses has ceased. If cycle dates are unknown, day 1 is the first of the calendar month. Use between 7:30 and 8:30 pm and upon waking. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Estradiol 6X, Estriol 6X, Folliculinum 6X, Belladonna 6C, Chelidonium Majus 6C, Glandula Suprarenalis Suis 6C, Hydrocortisone (Cortisol) 6C, Hypothalamus Suis 6C, Oophorinum (Suis) 6C, Pineal (Suis) 6C, Hypophysis (Suis) 6C, Sanguinaria Canadensis 6C, Lilium Tigrinum 12C, Pulsatilla (Vulgaris) 12C, Sepia 12C, Sulphur 12C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of hot flashes, climacteric complaints, ovarian complaints and pain, liver complaints, depression, menses scanty; stopped or late, irritable, uterine and vaginal complaints.

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. Administer orally, day 1 through 24 of the monthly menstrual cycle, even if menses has ceased. If cycle dates are unknown, day 1 is the first of the calendar month. Use between 7:30 and 8:30 pm and upon waking. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of hot flashes, climacteric complaints, ovarian complaints and pain, liver complaints, depression, menses scanty; stopped or late, irritable, uterine and vaginal complaints.

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., Ste. 169

Oxnard, CA 93035

www.wellnesscenter.net

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 50181-0067-1

EndoPure

by Theresa Dale, Ph.D, CCN

Homeopathic

ESTRO

HORMONE REJUVENATION SYSTEM

1 FL OZ (30 ml)

EndoPure EstroEndoPure Estro

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50181-0067-12025-06-06C16284748780-1ba0f9c33-3a95-a910-e053-dadaa90a0b85Drug Facts:
50181-0067-12021-01-29C16284748780-1ba0f9c33-3a95-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
50181-006750181-0067-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
2f59c551-ba24-47b5-b83c-009b2661f791a74e0bd3-061f-49f2-bd7f-31ffed0419312025-06-06WarningsExact identifier
spl id: 2f59c551-ba24-47b5-b83c-009b2661f791
spl set id: a74e0bd3-061f-49f2-bd7f-31ffed041931

Reported adverse events (FAERS/openFDA)#

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