Home NDC 48951-2062 Betonica Rosmarinus
Product NDC 48951-2062
11-digit product format 489512062
Labeler code 48951
Product ID 48951-2062_2c524d29-133e-1adc-e063-6294a90a305a
Type HUMAN OTC DRUG
Nonproprietary name Betonica Rosmarinus
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance STACHYS OFFICINALIS; ROSMARINUS OFFICINALIS FLOWERING TOP
Active strength 3; 3 [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 Betonica Rosmarinus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength STACHYS OFFICINALIS 3 [hp_X]/mL ROSMARINUS OFFICINALIS FLOWERING TOP 3 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination UO9989Y17N Internal UNII lookup 8JM482TI79 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 48951-2062-1 Betonica Rosmarinus 10 in 1 BOX LIQUID 10 4 48951-2062-1 Betonica Rosmarinus 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 48951-2062 BETONICA ROSMARINUS LIQUID [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 2 package rows 20250124_329763c8-92aa-4c61-9599-9ae183db239e.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 48951-2062-1 48951206201 10 AMPULE in 1 BOX (48951-2062-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current