Home NDC 48951-4199 Fragaria Vitis
Product NDC 48951-4199
11-digit product format 489514199
Labeler code 48951
Product ID 48951-4199_3dfc7c2e-22ed-0fa5-e063-6394a90a05ba
Type HUMAN OTC DRUG
Nonproprietary name Fragaria Vitis
Dosage form TABLET
Route ORAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance FRAGARIA VESCA WHOLE; VITIS VINIFERA LEAF
Active strength 1; 1 [hp_X]/1; [hp_X]/1
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 Fragaria Vitis
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FRAGARIA VESCA WHOLE 1 [hp_X]/1 VITIS VINIFERA LEAF 1 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5J340B7H82 Internal UNII lookup R1H893D80E 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 48951-4199-4 Fragaria Vitis 50 in 1 BOTTLE, GLASS TABLET 50 2
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 48951-4199-4 48951419904 50 TABLET in 1 BOTTLE, GLASS (48951-4199-4) 50 tablet 2009-09-01 No No Current