FDA.reportPublic FDA data

Endometrium Argentum

Product NDC
48951-4201
Requested package NDC
48951-4201-2
11-digit product format
489514201
Labeler code
48951
Product ID
48951-4201_43f90631-d1da-99c3-e063-6394a90a367b
Type
HUMAN OTC DRUG
Nonproprietary name
Endometrium Argentum
Dosage form
PELLET
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ECHINACEA, UNSPECIFIED; SILVER; BEEF; SILICON DIOXIDE
Active strength
2; 30; 30; 30 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Meat Proteins [EXT], Non-Standardized Food Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Endometrium Argentum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ECHINACEA, UNSPECIFIED2 [hp_X]/1
SILVER30 [hp_X]/1
BEEF30 [hp_X]/1
SILICON DIOXIDE30 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4N9P6CC1DXInternal UNII lookup
3M4G523W1GInternal UNII lookup
4PIB2155QPInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
5590d577-3a98-49b8-bb12-ddd7f5cfd080Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4201-2Endometrium Argentum1350 in 1 BOTTLE, GLASSPELLET13503

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BEEFACTIVE INGREDIENT4PIB2155QPENDOMETRIUM ARGENTUM SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1
COLLOIDAL SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU4ENDOMETRIUM ARGENTUM SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1
ECHINACEA, UNSPECIFIEDACTIVE INGREDIENT4N9P6CC1DXENDOMETRIUM ARGENTUM SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1
SILVERACTIVE INGREDIENT3M4G523W1GENDOMETRIUM ARGENTUM SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1
BEEFACTIVE MOIETY4PIB2155QPENDOMETRIUM ARGENTUM SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU4ENDOMETRIUM ARGENTUM SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1
ECHINACEA, UNSPECIFIEDACTIVE MOIETY4N9P6CC1DXENDOMETRIUM ARGENTUM SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1
SILVERACTIVE MOIETY3M4G523W1GENDOMETRIUM ARGENTUM SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ENDOMETRIUM ARGENTUM SPECIAL ORDER PELLET [URIEL PHARMACY INC.]1

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
Endometrium ArgentumENDOMETRIUM ARGENTUMUriel Pharmacy Inc.5590d577-3a98-49b8-bb12-ddd7f5cfd0802025-11-19WarningsExact identifier
ndc (package): 48951-4201-2
ndc (product): 48951-4201
ndc11 (package): 48951420102

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
48951-4201-2489514201021350 PELLET in 1 BOTTLE, GLASS (48951-4201-2) 1350 pellet2009-09-01NoNoCurrent