NDC 70663-008-01 - XR CELLULAR MAGIC

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: 70663-008
Requested NDC: 70663-008-01
Package NDCs from labels: 70663-008-01, 70663-008-02
Manufacturer: MESO SYSTEM S.A.
Effective date: 2016-12-17
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
XR CELLULAR MAGIC	MESO SYSTEM S.A.	2016-12-17	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70663-008-02	2020-01-31	C162847	48780-1	9d75b9d0-7054-f424-e053-dadaa90a57ce	XR CELLULAR MAGIC

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70663-008-01	XR CELLULAR MAGIC	50 mL in 1 BOTTLE	GEL	50		1
70663-008-02	XR CELLULAR MAGIC	1 in 1 BOX	GEL	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70663-008	XR CELLULAR MAGIC (SODIUM HYALURONATE) GEL [MESO SYSTEM S.A.]	1	Legacy NDC, 2 package rows	20161229_43e51c3c-add2-3f98-e054-00144ff88e88.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 10 of 10 · 182 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
43e51c3c-add3-3f98-e054-00144ff88e88			43e51c3c-add2-3f98-e054-00144ff88e88	2016-12-17	Warnings	Exact identifier spl id: 43e51c3c-add3-3f98-e054-00144ff88e88 spl set id: 43e51c3c-add2-3f98-e054-00144ff88e88
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.