Home NDC 48951-2054 Berberis Quartz
Product NDC 48951-2054
11-digit product format 489512054
Labeler code 48951
Product ID 48951-2054_48865336-9809-4f14-e063-6294a90a7c58
Type HUMAN OTC DRUG
Nonproprietary name Berberis Quartz
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance BERBERIS VULGARIS ROOT BARK; BOS TAURUS NASAL MUCOSA; SILICON DIOXIDE
Active strength 3; 7; 20 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
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 Berberis Quartz
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL BOS TAURUS NASAL MUCOSA 7 [hp_X]/mL SILICON DIOXIDE 20 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1TH8Q20J0U Internal UNII lookup 343455G79K Internal UNII lookup ETJ7Z6XBU4 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 48951-2054-1 Berberis Quartz 10 in 1 BOX LIQUID 10 5 48951-2054-1 Berberis Quartz 1 mL in 1 AMPULE LIQUID 1 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-2054 BERBERIS QUARTZ LIQUID [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 2 package rows 20240216_5da48d70-1140-495d-b672-0e55c04196e1.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 48951-2054-1 48951205401 10 AMPULE in 1 BOX (48951-2054-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current