NDC 52257-1370-01 - ATOMY PROPOLIS TOOTHPAS TE 200G

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: 52257-1370
Requested NDC: 52257-1370-01
Package NDCs from labels: 52257-1370-1, 52257-1370-2, 52257-1370-01
Manufacturer: ATOMY CO., LTD. | Kolmar Korea Co.,LTD. Gwanjeong 2 factory
Effective date: 2024-01-30
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
FLUORIDE ION - ATOMY CO., LTD. \| Kolmar Korea Co.,LTD. Gwanjeong 2 factory	ATOMY CO., LTD. \| Kolmar Korea Co.,LTD. Gwanjeong 2 factory	2024-01-30	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52257-1370-1	ATOMY PROPOLIS TOOTHPAS TE 200G	200 g in 1 TUBE	PASTE, DENTIFRICE	200		5
52257-1370-2	ATOMY PROPOLIS TOOTHPAS TE 200G	1 in 1 CARTON	PASTE, DENTIFRICE	1		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52257-1370	ATOMY PROPOLIS TOOTHPAS TE 200G (SODIUM MONOFLUOROPHOSPHATE, SODIUM FLUORIDE) PASTE, DENTIFRICE [ATOMY CO., LTD.]	5	Current NDC, Legacy NDC, 2 package rows	20240130_98aebbec-aec0-1478-e053-2a95a90a03ea.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 35 of 107 · 2,128 matching rows.

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Crest Pro Health Gum Detoxify and Restore Pro Whitening	STANNOUS FLUORIDE	The Procter & Gamble Manufacturing Company	f4d65b58-9818-820d-e053-2995a90a9f00	2026-01-08	Warnings	Exact identifier application number: M021
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Crest Complete Plus Scope Outlast	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	b6f9a813-7ed6-895c-e053-2995a90a9ea6	2026-01-08	Warnings	Exact identifier application number: M021 unii: 8ZYQ1474W7
Crest Premium Plus Scope Dual Blast Active Foam	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	b788d16a-8a58-0352-e053-2a95a90a965e	2026-01-08	Warnings	Exact identifier application number: M021 unii: 8ZYQ1474W7
Crest Premium Plus Scope Outlast Active Foam	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	b789587e-7f49-163a-e053-2a95a90a823f	2026-01-08	Warnings	Exact identifier application number: M021 unii: 8ZYQ1474W7
Crest Premium Plus Advanced Whitening Active Foam	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	b81a22dc-b759-24cd-e053-2995a90a9148	2026-01-08	Warnings	Exact identifier application number: M021 unii: 8ZYQ1474W7
Crest Premium Plus Deep Clean Active Foam	SODIUM FLUORIDE	The Procter & Gamble Manufacturing Company	b851fe5c-d904-12da-e053-2a95a90a86f9	2026-01-08	Warnings	Exact identifier application number: M021 unii: 8ZYQ1474W7
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Reported adverse events (FAERS/openFDA)#

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