NDC 60565-015-01 - Cellisys EX EGF Wrinkle 29 Activator

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
60565-015
Requested NDC
60565-015-01
Package NDCs from labels
60565-015-01, 60565-015-02
Manufacturer
DN Company Co., Ltd. | Cosmax, Inc.
Effective date
2019-03-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Cellisys EX EGF Wrinkle 29 Activator - DN Company Co., Ltd. | Cosmax, Inc.DN Company Co., Ltd. | Cosmax, Inc.2019-03-21HUMAN OTC DRUG LABEL

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 54 of 54 · 1,063 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
AntacidALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE AND SIMETHICONESafewayd36b56a4-06f0-47ff-8add-4c327d60be222016-01-21WarningsExact identifier
unii: 92RU3N3Y1O
Gas ReliefSIMETHICONESafeway14a9fb00-707a-4b55-a060-82ad53a806e32016-01-08WarningsExact identifier
unii: 92RU3N3Y1O

Reported adverse events (FAERS/openFDA)#

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