NDC 69153-080-01 - AN ADC SP INTENSIVE MOISTURE ESSENCE

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: 69153-080
Requested NDC: 69153-080-01
Package NDCs from labels: 69153-080-01, 69153-080-02
Manufacturer: AN Co Ltd.
Effective date: 2016-06-24
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
AN ADC SP INTENSIVE MOISTURE ESSENCE - AN Co Ltd.	AN Co Ltd.	2016-06-24	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69153-080-02	2023-01-30	C162847	48780-1	f386c649-bed8-0266-e053-dadaa90a7c1a	80861d31-100a-4c97-b9c7-afc3d8b3371a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69153-080-01	AN ADC SP INTENSIVE MOISTURE ESSENCE	55 g in 1 BOTTLE, PUMP	CREAM	55		1
69153-080-02	AN ADC SP INTENSIVE MOISTURE ESSENCE	1 in 1 CARTON	CREAM	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69153-080	AN ADC SP INTENSIVE MOISTURE ESSENCE (NIACINAMIDE) CREAM [AN CO LTD.]	1	Legacy NDC, 2 package rows	20160624_80861d31-100a-4c97-b9c7-afc3d8b3371a.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 18 of 18 · 343 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
9a5141e2-b665-429e-b13d-82a7e84779b4			80861d31-100a-4c97-b9c7-afc3d8b3371a	2016-06-24	Warnings	Exact identifier spl id: 9a5141e2-b665-429e-b13d-82a7e84779b4 spl set id: 80861d31-100a-4c97-b9c7-afc3d8b3371a
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.