Home NDC 48951-8435-3 Sambucus comp.
Product NDC 48951-8435
Requested package NDC 48951-8435-3
11-digit product format 489518435
Labeler code 48951
Product ID 48951-8435_36ea2222-8edc-156d-e063-6394a90a2866
Type HUMAN OTC DRUG
Nonproprietary name Sambucus comp.
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance SAMBUCUS NIGRA FLOWERING TOP; TEUCRIUM SCORODONIA WHOLE; BERBERIS VULGARIS ROOT BARK; PHOSPHORUS
Active strength 3; 4; 6; 6 [hp_X]/mL; [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 Sambucus comp.
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SAMBUCUS NIGRA FLOWERING TOP 3 [hp_X]/mL TEUCRIUM SCORODONIA WHOLE 4 [hp_X]/mL BERBERIS VULGARIS ROOT BARK 6 [hp_X]/mL PHOSPHORUS 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 48951-8435-3 Sambucus comp. 60 mL in 1 BOTTLE, DROPPER LIQUID 60 1
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 Sample Exclude flag Status 48951-8435-3 48951843503 60 mL in 1 BOTTLE, DROPPER (48951-8435-3) 60 ml 2009-09-01 No No Current