NDC 69255-500-01 - Doctor 9020 Dental Clinic

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: 69255-500
Requested NDC: 69255-500-01
Package NDCs from labels: 69255-500-01, 69255-500-02
Manufacturer: JANGIN PHARM CO.,LTD.
Effective date: 2019-12-15
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Doctor 9020 Dental Clinic - JANGIN PHARM CO.,LTD.	JANGIN PHARM CO.,LTD.	2019-12-15	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69255-500-02	2021-01-29	C162847	48780-1	ba0f9c33-20a5-a910-e053-dadaa90a0b85	99ca7d9b-44c0-b1ac-e053-2995a90aecd8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69255-500-01	Doctor 9020 Dental Clinic	12 mL in 1 POUCH	LIQUID	12		1
69255-500-02	Doctor 9020 Dental Clinic	15 in 1 PACKAGE	LIQUID	15		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69255-500	DOCTOR 9020 DENTAL CLINIC (SODIUM FLUORIDE) LIQUID [JANGIN PHARM CO.,LTD.]	1	Legacy NDC, 2 package rows	20191216_99ca7d9b-44c0-b1ac-e053-2995a90aecd8.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 56 of 56 · 1,105 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: VCQ006KQ1E
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

Reported adverse events (FAERS/openFDA)#

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