Home NDC 48951-8051-3 Plumbum 30
Product NDC 48951-8051
Requested package NDC 48951-8051-3
11-digit product format 489518051
Labeler code 48951
Product ID 48951-8051_36eb7fd7-43c0-bb2a-e063-6394a90acb76
Type HUMAN OTC DRUG
Nonproprietary name Plumbum 30
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance LEAD
Active strength 30 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Plumbum 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LEAD 30 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2P299V784P Internal UNII lookup
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 48951-8051-3 Plumbum 30 60 mL in 1 BOTTLE, DROPPER LIQUID 60 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8051 PLUMBUM 30 LIQUID [URIEL PHARMACY INC.] 2 Current NDC, Legacy NDC, 1 package rows 20201224_b637669a-17fb-ac23-e053-2a95a90af59f.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 48951-8051-3 48951805103 60 mL in 1 BOTTLE, DROPPER (48951-8051-3) 60 ml 2009-09-01 0000-00-00 No No Current