NDC 52257-1003-1 - ATOMY TOOTHPASTE

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: 52257-1003
Requested NDC: 52257-1003-1
Package NDCs from labels: 52257-1003-1, 52257-1003-2
Manufacturer: ATOMY CO LTD
Effective date: 2010-05-25
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
ATOMY TOOTHPASTE - ATOMY CO LTD	ATOMY CO LTD	2010-05-25	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52257-1003-2	2020-11-03	C162847	48780-1	956f9ecf-c73b-621f-e053-dbdaa90a74ad	ATOMY TOOTHPASTE
52257-1003-2	2019-10-21	C162847	48780-1	956f9ecf-c73b-621f-e053-dbdaa90a74ad	ATOMY TOOTHPASTE

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SODIUM FLUORIDE	ACTIVE INGREDIENT	8ZYQ1474W7	ATOMY TOOTHPASTE (SODIUM FLUORIDE) PASTE, DENTIFRICE [ATOMY CO LTD]	2
SODIUM MONOFLUOROPHOSPHATE	ACTIVE INGREDIENT	C810JCZ56Q	ATOMY TOOTHPASTE (SODIUM FLUORIDE) PASTE, DENTIFRICE [ATOMY CO LTD]	2
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	ATOMY TOOTHPASTE (SODIUM FLUORIDE) PASTE, DENTIFRICE [ATOMY CO LTD]	2

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 59 of 60 · 1,184 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ionite R	SODIUM FLUORIDE	Dharma Research, Inc.	1009afc7-6e9d-417f-a702-f8a941e08484	2020-11-06	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
Ionite R	SODIUM FLUORIDE	Dharma Research, Inc.	0e7b3eb3-3a9e-4a51-b2b5-9f36876fc8a5	2020-11-06	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
68093d0f-63ac-428f-82d9-03f71d835fc1			9497c229-2e43-4acf-b53c-be77d6831b6c	2020-11-02	Warnings	Exact identifier spl set id: 9497c229-2e43-4acf-b53c-be77d6831b6c
Ionite APF Foam	SODIUM FLUORIDE	Dharma Research, inc.	d22afac7-45d6-467e-951a-e7c241b9180d	2020-10-27	Warnings	Exact identifier unii: 8ZYQ1474W7
Ionite APF Foam	SODIUM FLUORIDE	Dharma Research, inc.	4828b482-486f-4105-bed0-3fe2ddbbddb1	2020-10-27	Warnings	Exact identifier unii: 8ZYQ1474W7
Ionite APF Foam	SODIUM FLUORIDE	Dharma Research, Inc.	8987b447-3fa3-4f52-aecc-80e44c981aaa	2020-10-27	Warnings	Exact identifier unii: 8ZYQ1474W7
Ionite APF Neutral	SODIUM FLUORIDE	Dharma Research, inc.	8191554f-adb6-4ba9-aa80-0a9bb65193ec	2020-10-27	Warnings	Exact identifier unii: 8ZYQ1474W7
Ionite APF Foam	SODIUM FLUORIDE	Dharma Research, inc.	ddd34623-cb79-4fa7-bd01-19122470b63d	2020-10-27	Warnings	Exact identifier unii: 8ZYQ1474W7
FluoriMax 5000	1.1% SODIUM FLUORIDE TOOTHPASTE	Elevate Oral Care	ae45ae2d-a21f-0a05-e053-2995a90a4d5e	2020-09-01	Warnings	Exact identifier unii: 8ZYQ1474W7
FluoriMax 5000 Sensitive	1.1% SODIUM FLUORIDE WITH 5% POTASSIUM NITRATE TOOTHPASTE	Elevate Oral Care	ae32b0a2-e42f-6a56-e053-2a95a90a0b00	2020-08-31	Warnings	Exact identifier unii: 8ZYQ1474W7
Sodium Fluoride 5000 ppm Sensitive	SODIUM FLUORIDE1.1%, POTASSIUM NITRATE 5%	Sheffield Pharmaceuticals LLC	02f4cf0b-188c-4522-b759-ffe4a9d150e8	2020-04-01	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
PreviDent 5000 Sensitive	SODIUM FLUORIDE AND POTASSIUM NITRATE	Colgate Oral Pharmaceuticals, Inc.	b028cfff-4946-49e8-b8bb-197ab99d0d35	2019-12-09	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
Colgate Max Fresh Cool Mint	SODIUM FLUORIDE	Mission Hills S.A de C.V	d142e43f-415a-41c5-a7db-8b18a039a323	2019-04-09	Warnings	Exact identifier unii: 8ZYQ1474W7
KOLORZ SIXTY SECOND FLUORIDE TRIPLE MINT	SODIUM FLUORIDE	DMG AMERICA, LLC	21fa26f2-0162-4044-aec0-d5360be3f3e0	2019-03-28	Warnings	Exact identifier unii: 8ZYQ1474W7
FLUORIDEX	SODIUM FLUORIDE	DEN-MAT HOLDINGS, LLC.	5fd60635-4b66-15e3-e053-2991aa0ab23a	2019-02-28	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
Pro-Den Rx	SODIUM FLUORIDE	Den-mat Holdings, Llc	e39b19f7-2b3e-4c77-9544-623ebad84870	2019-02-28	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
FLUORIDEX	SODIUM FLUORIDE	DEN-MAT HOLDINGS, LLC.	6014c330-3698-027c-e053-2a91aa0a64e5	2019-02-28	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
Plus White	SODIUM MONOFLUOROPHOSPHATE	CCA Industries, Inc.	7581b27b-6acb-45b0-8804-b5dae3498931	2018-08-01	Warnings	Exact identifier unii: C810JCZ56Q
Pro-Den Rx	SODIUM FLUORIDE	Den-Mat Holdings, Llc	ba020e07-ad41-4419-a503-f1245131b7d2	2018-04-17	Warnings, Adverse reactions	Exact identifier unii: 8ZYQ1474W7
Sensitive Tooth Polish	POTASSIUM NITRATE AND SODIUM FLUORIDE	Melaleuca, Inc.	689349e4-3980-a0e4-e053-2991aa0a9ef5	2018-03-29	Warnings	Exact identifier unii: 8ZYQ1474W7

Reported adverse events (FAERS/openFDA)#

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