NDC 72044-102-01 - CELDERMA Ninetalks Hydrogel Eye Patch

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: 72044-102
Requested NDC: 72044-102-01
Package NDCs from labels: 72044-102-01, 72044-102-02
Manufacturer: GENIC CO., LTD
Effective date: 2018-03-20
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
CELDERMA Ninetalks Hydrogel Eye Patch - GENIC CO., LTD	GENIC CO., LTD	2018-03-20	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72044-102-02	2022-01-28	C162847	48780-1	d6a99b39-343d-a426-e053-dadaa90af4c2	CELDERMA Ninetalks Hydrogel Eye Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72044-102-01	CELDERMA Ninetalks Hydrogel Eye Patch	4.7 g in 1 PATCH	PATCH	4.7		1
72044-102-02	CELDERMA Ninetalks Hydrogel Eye Patch	1 in 1 POUCH	PATCH	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72044-102	CELDERMA NINETALKS HYDROGEL EYE PATCH (GLYCERIN, NIACIN AMIDE, ADENOSINE) PATCH [GENIC CO., LTD]	1	Legacy NDC, 2 package rows	20180321_67dfb368-61c0-6c8d-e053-2991aa0aca3d.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 40 of 40 · 782 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eye Wash	WATER	CVS Pharmacy	049cee29-7ec2-4d5b-8308-f522acde43a7	2017-03-29	Warnings	Exact identifier unii: 059QF0KO0R
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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