Endometrium Argentum

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Endometrium Argentum
Generic name: ENDOMETRIUM ARGENTUM
Manufacturer: Uriel Pharmacy Inc
Product type: HUMAN OTC DRUG
SPL set ID: d2d1428a-c8b5-9529-e053-2995a90a2343
SPL ID: 59f6b1ae-0a3c-cf4d-e063-6294a90a0786
Version: 2
Effective date: 2026-08-26
Source export date: 2026-10-27
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:08:10

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Endometrium Argentum	openfda.brand_name
generic name		ENDOMETRIUM ARGENTUM	openfda.generic_name
manufacturer name		Uriel Pharmacy Inc	openfda.manufacturer_name
ndc	package	48951-4168-1	openfda.package_ndc
ndc	product	48951-4168	openfda.product_ndc
ndc11	package	48951416801	derived:openfda.package_ndc
spl id		59f6b1ae-0a3c-cf4d-e063-6294a90a0786	id
spl set id		d2d1428a-c8b5-9529-e053-2995a90a2343	set_id
unii		3M4G523W1G	openfda.unii
unii		4PIB2155QP	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		4N9P6CC1DX	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

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.

Reported adverse events (FAERS/openFDA)#

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