Home NDC 48951-8034 Plantago Primula
Product NDC 48951-8034
11-digit product format 489518034
Labeler code 48951
Product ID 48951-8034_2c522c57-994b-4e02-e063-6394a90a1f12
Type HUMAN OTC DRUG
Nonproprietary name Plantago Primula
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance PLANTAGO MAJOR LEAF; PRIMULA VERIS FLOWER; HYOSCYAMUS NIGER LEAF
Active strength 2; 2; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
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 Plantago Primula
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PLANTAGO MAJOR LEAF 2 [hp_X]/mL PRIMULA VERIS FLOWER 2 [hp_X]/mL HYOSCYAMUS NIGER LEAF 3 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 7DC28K241X Internal UNII lookup W5BET37294 Internal UNII lookup 32IT7G8BAW 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 48951-8034-1 Plantago Primula 10 in 1 BOX LIQUID 10 4 48951-8034-1 Plantago Primula 1 mL in 1 AMPULE LIQUID 1 4
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8034 PLANTAGO PRIMULA LIQUID [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 2 package rows 20250124_25545753-2d00-47fe-b318-b7e4a47c3d0d.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 48951-8034-1 48951803401 10 AMPULE in 1 BOX (48951-8034-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current