Progenite

AMMONIUM CARBONICUM, BARYTA MURIATICA, BORAX, CAULOPHYLLUM THALICTROIDES, NATRUM CARBONICUM, SABAL SERRULATA, SABINA, SULPHURICUM ACIDUM, THIOSINAMINUM, FOLLICULINUM, TUBA UTERINA SUIS, UTERUS SUIS, HYPOTHALAMUS (SUIS), THYROIDINUM (SUIS), AGNUS CASTUS, CONIUM MACULATUM, GRAPHITES, HYOSCYAMUS NIGER, SEPIA, SELENIUM METALLICUM, X-RAY ORAL HUMAN OTC DRUG

Progenite is an FDA drug label for the active ingredient AMMONIUM CARBONICUM, BARYTA MURIATICA, BORAX, CAULOPHYLLUM THALICTROIDES, NATRUM CARBONICUM, SABAL SERRULATA, SABINA, SULPHURICUM ACIDUM, THIOSINAMINUM, FOLLICULINUM, TUBA UTERINA SUIS, UTERUS SUIS, HYPOTHALAMUS (SUIS), THYROIDINUM (SUIS), AGNUS CASTUS, CONIUM MACULATUM, GRAPHITES, HYOSCYAMUS NIGER, SEPIA, SELENIUM METALLICUM, X-RAY manufactured by Deseret Biologicals administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231212.

Generic name
AMMONIUM CARBONICUM, BARYTA MURIATICA, BORAX, CAULOPHYLLUM THALICTROIDES, NATRUM CARBONICUM, SABAL SERRULATA, SABINA, SULPHURICUM ACIDUM, THIOSINAMINUM, FOLLICULINUM, TUBA UTERINA SUIS, UTERUS SUIS, HYPOTHALAMUS (SUIS), THYROIDINUM (SUIS), AGNUS CASTUS, CONIUM MACULATUM, GRAPHITES, HYOSCYAMUS NIGER, SEPIA, SELENIUM METALLICUM, X-RAY
Manufacturer
Deseret Biologicals
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
43742-1170
Application
N/A
Label effective
20231212

About this product

Progenite is an FDA-registered drug product whose active ingredient is AMMONIUM CARBONICUM, BARYTA MURIATICA, BORAX, CAULOPHYLLUM THALICTROIDES, NATRUM CARBONICUM, SABAL SERRULATA, SABINA, SULPHURICUM ACIDUM, THIOSINAMINUM, FOLLICULINUM, TUBA UTERINA SUIS, UTERUS SUIS, HYPOTHALAMUS (SUIS), THYROIDINUM (SUIS), AGNUS CASTUS, CONIUM MACULATUM, GRAPHITES, HYOSCYAMUS NIGER, SEPIA, SELENIUM METALLICUM, X-RAY. It is labelled by Deseret Biologicals taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 43742-1170, label effective 20231212. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing AMMONIUM CARBONICUM, BARYTA MURIATICA, BORAX, CAULOPHYLLUM THALICTROIDES, NATRUM CARBONICUM, SABAL SERRULATA, SABINA, SULPHURICUM ACIDUM, THIOSINAMINUM, FOLLICULINUM, TUBA UTERINA SUIS, UTERUS SUIS, HYPOTHALAMUS (SUIS), THYROIDINUM (SUIS), AGNUS CASTUS, CONIUM MACULATUM, GRAPHITES, HYOSCYAMUS NIGER, SEPIA, SELENIUM METALLICUM, X-RAY are most often described in connection with: homeopathic indications, temporary relief, symptoms related, impaired reproductive, hormonal imbalances, reduced sex, irregular menses, based upon. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

ACTIVE INGREDIENTS: Ammonium Carbonicum 6X, Baryta Muriatica 6X, Borax 6X, Caulophyllum Thalictroides 6X, Natrum Carbonicum 6X, Sabal Serrulata 6X, Sabina 6X, Sulphuricum Acidum 6X, Thiosinaminum 6X, Folliculinum 6X, 12X, 30X, Tuba Uterina Suis 6X, 12X, 30X, Uterus Suis 6X, 12X, 30X, Hypothalamus (Suis) 8X, 12X, 30X, Thyroidinum (Suis) 8X, 12X, 30X, Agnus Castus 8X, 12X, 30X, Conium Maculatum 12X, Graphites 12X, Hyoscyamus Niger 12X, Sepia 12X, Selenium Metallicum 12X, 30X, X-Ray 12X, 30X.

Indications & Usage

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to impaired reproductive activity in both males and females, such as hormonal imbalances, reduced sex drive, and irregular menses.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Dosage & Administration

DIRECTIONS: 1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Warnings

WARNINGS: Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

Frequently asked questions

What is Progenite used for?
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to impaired reproductive activity in both males and females, such as hormonal imbalances, reduced sex drive, and irregular menses.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Who makes Progenite?
Deseret Biologicals is the labeler of record for Progenite.

What form does Progenite come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Progenite prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has Progenite been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.