Home NDC 48951-8310 Polygonatum Cepa
Product NDC 48951-8310
11-digit product format 489518310
Labeler code 48951
Product ID 48951-8310_43d18929-b47b-3cf2-e063-6394a90a20f1
Type HUMAN OTC DRUG
Nonproprietary name Polygonatum Cepa
Dosage form GEL
Route TOPICAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ONION; ECHINACEA ANGUSTIFOLIA; HIRUDIN; POLYGONATUM CYRTONEMA ROOT; VESPA CRABRO; GOLD; BOS TAURUS CARTILAGE; COPPER; SUS SCROFA SKIN; BOS TAURUS PLACENTA; SILICON DIOXIDE; THUJA OCCIDENTALIS WHOLE; SILVER; BARIUM CITRATE; GRAPHITE
Active strength 2; 2; 4; 4; 6; 8; 8; 8; 8; 8; 8; 8; 12; 12; 17 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
Pharmacologic classes Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cells, Epidermal [EXT], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Animal Skin Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Standardized Chemical Allergen [EPC], Vegetable Proteins [CS]
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 Polygonatum Cepa
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ONION 2 [hp_X]/g ECHINACEA ANGUSTIFOLIA 2 [hp_X]/g HIRUDIN 4 [hp_X]/g POLYGONATUM CYRTONEMA ROOT 4 [hp_X]/g VESPA CRABRO 6 [hp_X]/g GOLD 8 [hp_X]/g BOS TAURUS CARTILAGE 8 [hp_X]/g COPPER 8 [hp_X]/g SUS SCROFA SKIN 8 [hp_X]/g BOS TAURUS PLACENTA 8 [hp_X]/g SILICON DIOXIDE 8 [hp_X]/g THUJA OCCIDENTALIS WHOLE 8 [hp_X]/g SILVER 12 [hp_X]/g BARIUM CITRATE 12 [hp_X]/g GRAPHITE 17 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 15 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-8310-5 Polygonatum Cepa 60 g in 1 TUBE GEL 60 7
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8310 POLYGONATUM CEPA GEL [URIEL PHARMACY INC.] 6 Current NDC, Legacy NDC, 1 package rows 20240210_6ba0ac36-16cc-49bd-b37f-90cf18acbd5a.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 Sample Exclude flag Status 48951-8310-5 48951831005 60 g in 1 TUBE (48951-8310-5) 60 g 2009-09-01 No No Current