ATOMY TOOTHPASTE

Manufacturer: ATOMY CO LTD
Effective date: 2010-05-25
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-02 01:53:05

Label at a glance#

ProductATOMY TOOTHPASTE

Active ingredientSODIUM FLUORIDE, SODIUM MONOFLUOROPHOSPHATE

Label structure2 sections

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
Sodium Monofluorophosphate 0.16%
Sodium Fluoride 0.1%

Uses
aid in the prevention of dental cavities

Directions

Adults and children 2 years of age and older
;Brush teeth throughly preferably after each meal or at least twice a day or as directed by a dentist or doctor.

Children under 6 years
;To minimize swallowing, use a pea-sized amount and supervise brushing until good habits are established.

Children under 2 years
;Consult a dentist or doctor.

Warnings

Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ATOMY TOOTHPASTE

200g/7.05 fl.oz

image of carton 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	SPL version
SODIUM FLUORIDE	ACTIVE INGREDIENT	8ZYQ1474W7	2
SODIUM MONOFLUOROPHOSPHATE	ACTIVE INGREDIENT	C810JCZ56Q	2
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

ATOMY TOOTHPASTE
SODIUM FLUORIDE
FLUORIDE ION
SODIUM MONOFLUOROPHOSPHATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52257-1003	52257-1003-1, 52257-1003-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM FLUORIDE	8ZYQ1474W7	ACTIB
SODIUM MONOFLUOROPHOSPHATE	C810JCZ56Q	ACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
68093d0f-63ac-428f-82d9-03f71d835fc1			9497c229-2e43-4acf-b53c-be77d6831b6c	2020-11-02	Warnings	Exact identifier spl set id: 9497c229-2e43-4acf-b53c-be77d6831b6c

Reported adverse events (FAERS/openFDA)#

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