Home NDC 48951-8178 Secale Quartz
Product NDC 48951-8178
11-digit product format 489518178
Labeler code 48951
Product ID 48951-8178_45778341-8034-7ccc-e063-6294a90a44a0
Type HUMAN OTC DRUG
Nonproprietary name Secale Quartz
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance SANGUINARIA CANADENSIS ROOT; CLAVICEPS PURPUREA SCLEROTIUM; SILICON DIOXIDE
Active strength 6; 6; 30 [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 Secale Quartz
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SANGUINARIA CANADENSIS ROOT 6 [hp_X]/mL CLAVICEPS PURPUREA SCLEROTIUM 6 [hp_X]/mL SILICON DIOXIDE 30 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination N9288CD508 Internal UNII lookup 01G9XEA93N Internal UNII lookup ETJ7Z6XBU4 Internal UNII lookup
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 48951-8178-1 Secale Quartz 10 in 1 BOX LIQUID 10 6 48951-8178-1 Secale Quartz 1 mL in 1 AMPULE LIQUID 1 6
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8178 SECALE QUARTZ LIQUID [URIEL PHARMACY INC.] 5 Current NDC, Legacy NDC, 2 package rows 20241213_1e9f55d7-22d5-4412-ac35-b4400bdf29a0.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 48951-8178-1 48951817801 10 AMPULE in 1 BOX (48951-8178-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current