NDC 55651-031 - Biomedic Artificial Tears

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: 55651-031
Package NDCs from labels: 55651-031-01
Manufacturer: KC Pharmaceuticals, Inc.
Effective date: 2025-12-31
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Biomedic Artificial Tears 15mL (MFR - EXPORT)	KC Pharmaceuticals, Inc.	2025-12-31	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55651-031-01	Biomedic Artificial Tears	1 in 1 CARTON	LIQUID	1		2
55651-031-01	Biomedic Artificial Tears	15 mL in 1 BOTTLE, PLASTIC	LIQUID	15		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55651-031	BIOMEDIC ARTIFICIAL TEARS (GLYCERIN, HYPROMELLOSE) LIQUID [KC PHARMACEUTICALS, INC.]	1	2 package rows	20230325_f7b178d7-c570-24a8-e053-6294a90adfdb.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 149 of 149 · 2,961 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Baxter Healthcare Corporation	f09f80bf-2f8b-4420-865d-aec2d5e5cd4d	2012-06-12		Exact identifier unii: 451W47IQ8X unii: 660YQ98I10

Reported adverse events (FAERS/openFDA)#

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