Home NDC 48951-3091-1 Cichorium Oxalis
Product NDC 48951-3091
Requested package NDC 48951-3091-1
11-digit product format 489513091
Labeler code 48951
Product ID 48951-3091_4bada4cc-42b1-239c-e063-6394a90a52cb
Type HUMAN OTC DRUG
Nonproprietary name Cichorium Oxalis
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance CICHORIUM INTYBUS WHOLE; OXALIS ACETOSELLA LEAF; ACTIVATED CHARCOAL; SUS SCROFA PANCREAS; BARIUM CITRATE; IRON
Active strength 3; 3; 6; 6; 10; 20 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE]
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 Cichorium Oxalis
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CICHORIUM INTYBUS WHOLE 3 [hp_X]/mL OXALIS ACETOSELLA LEAF 3 [hp_X]/mL ACTIVATED CHARCOAL 6 [hp_X]/mL SUS SCROFA PANCREAS 6 [hp_X]/mL BARIUM CITRATE 10 [hp_X]/mL IRON 20 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 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 48951-3091-1 Cichorium Oxalis 10 in 1 BOX LIQUID 10 4 48951-3091-1 Cichorium Oxalis 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 48951-3091 CICHORIUM OXALIS LIQUID [URIEL PHARMACY INC.] 3 Current NDC, Legacy NDC, 2 package rows 20240203_3d284b66-6a25-4d6f-9d37-e7642ae88d3b.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 48951-3091-1 48951309101 10 AMPULE in 1 BOX (48951-3091-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current