Home NDC 48951-4168 Endometrium Argentum
Product NDC 48951-4168
11-digit product format 489514168
Labeler code 48951
Product ID 48951-4168_59f6b1ae-0a3c-cf4d-e063-6294a90a0786
Type HUMAN OTC DRUG
Nonproprietary name Endometrium Argentum
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance BEEF; SILICON DIOXIDE; ECHINACEA, UNSPECIFIED; SILVER
Active strength 30; 30; 2; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
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 2027-12-31
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 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BEEF 30 [hp_X]/mL SILICON DIOXIDE 30 [hp_X]/mL ECHINACEA, UNSPECIFIED 2 [hp_X]/mL SILVER 30 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-4168-1 Endometrium Argentum 10 in 1 BOX LIQUID 10 1 48951-4168-1 Endometrium Argentum 1 mL in 1 AMPULE LIQUID 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-4168 ENDOMETRIUM ARGENTUM LIQUID [URIEL PHARMACY INC] 1 Current NDC, Legacy NDC, 2 package rows 20211212_d2d1428a-c8b5-9529-e053-2995a90a2343.zip
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 48951-4168-1 48951416801 10 AMPULE in 1 BOX (48951-4168-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current