NDC 72729-030-01 - reFACE TOX AMPULE

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: 72729-030
Requested NDC: 72729-030-01
Package NDCs from labels: 72729-030-01, 72729-030-02
Manufacturer: Woorhi Mechatronics Co., Ltd. | Ester Co., Ltd.
Effective date: 2021-06-28
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
reFACE TOX AMPULE - Woorhi Mechatronics Co., Ltd. \| Ester Co., Ltd.	Woorhi Mechatronics Co., Ltd. \| Ester Co., Ltd.	2021-06-28	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72729-030-02	2023-01-30	C162847	48780-1	f386c649-e72d-0266-e053-dadaa90a7c1a	f96eb0ae-67dd-4f3b-8e0b-36402dc1cfdc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72729-030-01	reFACE TOX AMPULE	3.5 mL in 1 CONTAINER	SOLUTION	3.5		2
72729-030-02	reFACE TOX AMPULE	4 in 1 CARTON	SOLUTION	4		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72729-030	REFACE TOX AMPULE (NIACINAMIDE, ADENOSINE) SOLUTION [WOORHI MECHATRONICS CO., LTD.]	2	Legacy NDC, 2 package rows	20210629_f96eb0ae-67dd-4f3b-8e0b-36402dc1cfdc.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 21 of 21 · 402 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
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.