ARU CAVITY PROTECTION

Manufacturer: Ashtel Studios, Inc.
Effective date: 2026-01-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:34:39

Label at a glance#

ProductARU CAVITY PROTECTION

Active ingredientSODIUM FLUORIDE

Label structure9 sections

Indications and uses

helps protect against cavities.

Dosage and administration

• Adults and children 3 years and older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist. • Do not swallow. • Children under 6 years: to minimize swallowing use a pea-sized amount and supervise children's brushing and rinsing until good habits are established. • Children under 2 years of age: Consult a dentist or doctor.

Contacts and useful links#

PhoneLabel contact1-877-274-8358

PhoneLabel contact1-909-434-0911

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.243%
(0.15% w/v fluoride ion)

Purpose

OTC - PURPOSE SECTION

Anticavity

Uses

INDICATIONS & USAGE SECTION

helps protect against cavities.

Warnings

WARNINGS SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children under 6 years of age. If you accidentally swallow more than used for brushing, seek professional help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

• Adults and children 3 years and older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist.
• Do not swallow.
• Children under 6 years: to minimize swallowing use a pea-sized amount and supervise children's brushing and rinsing until good habits are established.
• Children under 2 years of age: Consult a dentist or doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sorbitol, Silica, Aqua (Water), Cocamidopropyl Betaine, Flavor, Cellulose Gum, Potassium Sorbate, Stevia Rebaudiana Leaf Extract.

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free 1-877-274-8358

SPL UNCLASSIFIED SECTION

9 INGREDIENTS

WE DON'T DO SECRETS.
EVERY INGREDIENT
IS DECODED HERE.

DESIGNED IN U.S.A.
MADE IN INDIA

1-909-434-0911 INTERNATIONAL

PATENTS, COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE

DISTRIBUTED BY ASHTEL STUDIOS INC.
ONTARIO, CALIFORNIA 91761

GETARU.COM

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ARUCAVITYPROTECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
891775	sodium fluoride 0.243 % Toothpaste	PSN	1
891775	sodium fluoride 0.00243 MG/MG Toothpaste	SCD	1
891775	sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste	SY	1
891775	sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste	SY	1
891775	sodium fluoride 0.243 % (fluoride ion 0.15 % ) Toothpaste	SY	1
891775	sodium fluoride 0.243 % (fluoride ion 0.16 % ) Toothpaste	SY	1

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
QR code link	QR Code	getaru.com/products/cavity-protection-toothpaste		70108287-7.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70108-287-01	ARU CAVITY PROTECTION	99 g in 1 TUBE	PASTE, DENTIFRICE	99		1
70108-287-01	ARU CAVITY PROTECTION	1 in 1 BOX	PASTE, DENTIFRICE	1		1

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

ARU CAVITY PROTECTION
Sodium Fluoride
FLUORIDE ION
SORBITOL
SILICON DIOXIDE
WATER
COCAMIDOPROPYL BETAINE
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
POTASSIUM SORBATE
STEVIA REBAUDIANA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70108-287	70108-287-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM FLUORIDE	8ZYQ1474W7	ACTIB
SORBITOL	506T60A25R	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED	K679OBS311	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT
STEVIA REBAUDIANA LEAF	6TC6NN0876	IACT

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
ARU CAVITY PROTECTION	SODIUM FLUORIDE	Ashtel Studios, Inc.	97bd2934-4bff-4fdb-9199-fcdc0f77fada	2026-01-13	Warnings	Exact identifier ndc (package): 70108-287-01 ndc (product): 70108-287 ndc11 (package): 70108028701 spl id: a8dd9fac-df83-4382-8fed-ca4734926738 spl set id: 97bd2934-4bff-4fdb-9199-fcdc0f77fada

Reported adverse events (FAERS/openFDA)#

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