NDC 59078-314-01 - PANDAS DREAM SO COOL EYE SERUM

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: 59078-314
Requested NDC: 59078-314-01
Package NDCs from labels: 59078-314-01, 59078-314-02
Manufacturer: TONYMOLY CO.,LTD
Effective date: 2016-06-16
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
PANDAS DREAM SO COOL EYE SERUM - TONYMOLY CO.,LTD	TONYMOLY CO.,LTD	2016-06-16	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59078-314-02	2020-01-31	C162847	48780-1	9d75b9d0-415c-f424-e053-dadaa90a57ce	619376f9-7f33-4c8b-92ea-eae26d6b4069

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59078-314-01	PANDAS DREAM SO COOL EYE SERUM	9 g in 1 BOTTLE, PLASTIC	STICK	9		1
59078-314-02	PANDAS DREAM SO COOL EYE SERUM	1 in 1 CARTON	STICK	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59078-314	PANDAS DREAM SO COOL EYE SERUM (DIMETHICONE) STICK [TONYMOLY CO.,LTD]	1	Legacy NDC, 2 package rows	20160616_619376f9-7f33-4c8b-92ea-eae26d6b4069.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 · 781 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Gas Relief	SIMETHICONE	Safeway	14a9fb00-707a-4b55-a060-82ad53a806e3	2016-01-08	Warnings	Exact identifier unii: 92RU3N3Y1O

Reported adverse events (FAERS/openFDA)#

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