NDC 48951-4199-04 - Fragaria Vitis

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 48951-4199
Requested NDC: 48951-4199-04
Package NDCs from labels: 48951-4199-4, 48951-4199-04
Manufacturer: Uriel Pharmacy, Inc
Effective date: 2025-09-04
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Fragaria Vitis - Uriel Pharmacy, Inc	Uriel Pharmacy, Inc	2025-09-04	HUMAN OTC DRUG LABEL

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lycopodium Berberis	LYCOPODIUM BERBERIS	Uriel Pharmacy Inc.	8312ff6b-4d20-41d4-b736-b50c081c64b6	2025-10-30	Warnings	Exact identifier unii: R1H893D80E unii: 5J340B7H82
Fragaria Vitis	FRAGARIA VITIS	Uriel Pharmacy, Inc	26cf84e7-74fc-9199-e063-6394a90ad2bb	2025-09-04	Warnings	Exact identifier ndc (package): 48951-4199-4 ndc (product): 48951-4199 ndc11 (package): 48951419904 spl id: 3dfc7c2e-22ed-0fa5-e063-6394a90a05ba spl set id: 26cf84e7-74fc-9199-e063-6394a90ad2bb unii: R1H893D80E unii: 5J340B7H82

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.