NDC 0273-8010-01 - NAFRINSE PACKETSKIT VERY BERRY

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: 0273-8010
Requested NDC: 0273-8010-01
Package NDCs from labels: 0273-8010-01, 0273-8010-02
Manufacturer: Young Dental Manufacturing Co 1, LLC. | Medical Products Laboratories, Inc
Effective date: 2018-12-14
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
NAFRINSE PACKETSKIT VERY BERRY - Young Dental Manufacturing Co 1, LLC. \| Medical Products Laboratories, Inc	Young Dental Manufacturing Co 1, LLC. \| Medical Products Laboratories, Inc	2018-12-14	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0273-8010-02	2020-01-31	C162847	48780-1	9d75b9d0-c3d0-f424-e053-dadaa90a57ce	Convinience KIT -20 pack of Nafrinse packets, a polyethylene jug, dispenser pump, plastic cups, paper napkins, and trash bag with ties

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0273-8010-01	NAFRINSE PACKETSKIT VERY BERRY	3 g in 1 PACKET	POWDER	3		2
0273-8010-02	NAFRINSE PACKETSKIT VERY BERRY	20 in 1 KIT	POWDER	20		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0273-8010	NAFRINSE PACKETSKIT VERY BERRY (SODIUM FLUORIDE) POWDER [YOUNG DENTAL MANUFACTURING CO 1, LLC.]	2	Legacy NDC, 2 package rows	20181215_97f64104-21b1-4fb3-a9d4-f1c17b8ae2b4.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 57 of 57 · 1,126 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Homeoplex D	GLYCERINUM, PHYTOLACCA DECANDRA, TARAXACUM OFFICINALE, ARSENICUM ALBUM, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETYLSALICYLICUM ACIDUM, GLONOINUM, INSULINUM (SUIS), LITHIUM CARBONICUM, THYROIDINUM (SUIS), SALICYLICUM ACIDUM, ADRENOCORTICOTROPHIN, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE, SORBITOL, RESORCINUM, BENZYL ALCOHOL, LACTICUM ACIDUM, ISOPROPYL PALMITATE, BORICUM ACIDUM, ACETICUM ACIDUM,	Supplement Clinic, LLC.	cd6b48ab-3566-484d-8deb-15ef6f8e7e8f	2017-11-01	Warnings	Exact identifier unii: 1VPU26JZZ4
SF	1.1% SODIUM FLUORIDE	Cypress Pharmaceutical, Inc.	b7c0a768-7e8a-40b9-876f-b86d3dc5e848	2016-07-06	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
SF 5000 Plus	1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM	Cypress Pharmaceutical, Inc.	fa625ece-d873-491a-8d45-2833b64e5425	2016-07-01	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
Ionite H	SODIUM FLUORIDE, POTASSIUM NITRATE	Dharma Research, Inc.	54c1a27c-5936-4ee2-a419-3891d3df9745	2015-08-02	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
Ionite H	SODIUM FLUORIDE, POTASSIUM NITRATE	Dharma Research, Inc.	642fec99-c5c5-4ef2-986e-5b5f7cf460de	2015-08-02	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	051f7347-5a76-4664-8fe2-e61b3dfcb0e4	2014-08-27		Exact identifier unii: XF417D3PSL

Reported adverse events (FAERS/openFDA)#

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