Endometrium Argentum

Endometrium Argentum is an FDA-registered drug product whose active ingredient is ENDOMETRIUM ARGENTUM. It is labelled by Uriel Pharmacy Inc taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 48951-4168, label effective 20260826. 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.

FOR ORAL USE ONLY

Directions: Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow. Follow inside instructions to open ampule.

Warnings: NOT FOR INJECTION Do not use if allergic to any ingredient. Consult a physician if symptoms worsen. If pregnant or nursing, consult a physician before use. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

What is Endometrium Argentum used for?
FOR ORAL USE ONLY

Who makes Endometrium Argentum?
Uriel Pharmacy Inc is the labeler of record for Endometrium Argentum.

What form does Endometrium Argentum 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 Endometrium Argentum 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 Endometrium Argentum 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.