Dry Eye Test

Product NDC: 51801-008
11-digit product format: 518010008
Labeler code: 51801
Product ID: 51801-008_7490418c-b489-4b90-bc3d-33ed71231e2d
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Fluorescein Sodium
Dosage form: STRIP
Route: OPHTHALMIC
Labeler: Nomax Inc.
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2013-12-05
Substance: FLUORESCEIN SODIUM
Active strength: .12 mg/1
Pharmacologic classes: Diagnostic Dye [EPC], Dyes [MoA]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Dry Eye Test
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
FLUORESCEIN SODIUM	.12 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
93X55PE38X	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
04866053-f973-471e-b3bc-241fb76303a2	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
8f43a274-9585-47cb-b427-0eb3e578384d	Product name	1	20250623
4a998fa9-995e-4ea5-97ef-93a559305758	Product name	1	20200706
c94ccba7-2a03-4a3e-a891-d62a57340fb2	Product name	1	20180215

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51801-008-15	Dry Eye Test	2 in 1 POUCH	STRIP	2		3
51801-008-15	Dry Eye Test	50 in 1 CARTON	STRIP	50		3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
Fluorescein Sodium	ACTIVE INGREDIENT	93X55PE38X	DRY EYE TEST (FLUORESCEIN SODIUM) STRIP [NOMAX INC.]	1
FLUORESCEIN	ACTIVE MOIETY	TPY09G7XIR	DRY EYE TEST (FLUORESCEIN SODIUM) STRIP [NOMAX INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51801-008	DRY EYE TEST (FLUORESCEIN SODIUM) STRIP [NOMAX INC.]	3	Current NDC, Legacy NDC, 2 package rows	20191224_04866053-f973-471e-b3bc-241fb76303a2.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dry Eye Test	FLUORESCEIN SODIUM	Nomax Inc.	04866053-f973-471e-b3bc-241fb76303a2	2019-12-23		Exact identifier ndc (product): 51801-008

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
93X55PE38X	FLUORESCEIN SODIUM	518-47-8	FLUORESCEIN SODIUM

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
51801-008-15	51801000815	50 POUCH in 1 CARTON (51801-008-15) / 2 STRIP in 1 POUCH	50 pouch	2013-12-05	0000-00-00	No	No	Current