Home NDC 48951-8442 Prunus spinosa et summ. 30
Product NDC 48951-8442
11-digit product format 489518442
Labeler code 48951
Product ID 48951-8442_4d7a43b0-f915-e35b-e063-6294a90a0ed3
Type HUMAN OTC DRUG
Nonproprietary name Prunus spinosa et summ. 30
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance SLOE
Active strength 1 [hp_X]/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Prunus spinosa et summ. 30
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SLOE 1 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3MLB4858X7 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 48951-8442-3 Prunus spinosa et summ. 30 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 48951-8442-3 48951844203 60 mL in 1 BOTTLE, DROPPER (48951-8442-3) 60 ml 2009-09-01 No No Current