NDC 70592-010-01 - FREEZE 24 7 RADIANCE BRIGHTENING FACE MASK

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: 70592-010
Requested NDC: 70592-010-01
Package NDCs from labels: 70592-010-01, 70592-010-02
Manufacturer: Summit C&T LLC | SANSUNG LIFE & SCIENCE CO., LTD.
Effective date: 2016-04-07
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Witch Hazel - Summit C&T LLC \| SANSUNG LIFE & SCIENCE CO., LTD.	Summit C&T LLC \| SANSUNG LIFE & SCIENCE CO., LTD.	2016-04-07	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70592-010-02	2020-01-31	C162847	48780-1	9d75b9d0-4bb2-f424-e053-dadaa90a57ce	a7220f6c-9cba-4514-b702-fda9e60185d4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70592-010-01	FREEZE 24 7 RADIANCE BRIGHTENING FACE MASK	30 mL in 1 CELLO PACK	PATCH	30		1
70592-010-02	FREEZE 24 7 RADIANCE BRIGHTENING FACE MASK	1 in 1 CARTON	PATCH	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70592-010	FREEZE 24 7 RADIANCE BRIGHTENING FACE MASK (WITCH HAZEL) PATCH [SUMMIT C&T LLC]	1	Legacy NDC, 2 package rows	20160407_a7220f6c-9cba-4514-b702-fda9e60185d4.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 15 of 15 · 282 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
362ca40f-ac01-4b06-97f1-6b9f0ad863dd			a7220f6c-9cba-4514-b702-fda9e60185d4	2016-04-07	Warnings	Exact identifier spl id: 362ca40f-ac01-4b06-97f1-6b9f0ad863dd spl set id: a7220f6c-9cba-4514-b702-fda9e60185d4

Reported adverse events (FAERS/openFDA)#

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