EverSmile Squirt Foaming Mouthwash - Bubble Gum

Manufacturer
Everbrands, Inc.
Effective date
2026-04-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:54:30

Label at a glance#

ProductEverSmile Squirt
Active ingredientSODIUM FLUORIDE
Label structure10 sections

Indications and uses

•aids in the prevention of dental cavities

Dosage and administration

adults and children 6 years of age and older: • use once a day after brushing your teeth with   a toothpaste • pump 1 mL of product (4 pumps) into your mouth and • swish rinse between your teeth for 1 minute and then • spit out • do not swallow the rinse • do not eat or drink for 30 minutes after rinsing • instruct children under 12 years of age in good rinsing   habits (to minimize swallowing) • supervise childre...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.05% (0.02% w/v)

Purpose

OTC - PURPOSE SECTION

Anticavity

Uses

INDICATIONS & USAGE SECTION

•aids in the prevention of dental cavities


​​Warnings

WARNINGS SECTION

Stop use and ask dentist if oral irritation or tooth

sensitivity occurs

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If more than used for rinsing is accidentally

swallowed, get medical help or contact a

Poison Control Center right away.

​Directions:

DOSAGE & ADMINISTRATION SECTION

adults and children 6 years of age and older:

• use once a day after brushing your teeth with

  a toothpaste

• pump 1 mL of product (4 pumps) into your mouth and

• swish rinse between your teeth for 1 minute and then

• spit out

• do not swallow the rinse

• do not eat or drink for 30 minutes after rinsing

• instruct children under 12 years of age in good rinsing

  habits (to minimize swallowing)

• supervise children as necessary until capable of using

  without supervision

•Children under 6 years of age: consult a dentist or

  doctor

Other information

OTHER SAFETY INFORMATION

store at controlled room

temperature 68-77°F(20-25°)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, hydrogen peroxide, PVP, PEG, glycerin, sucralose,
sodium lauryl sulfate, natural bubble gum flavor, sodium
citrate, sodium benzoate

OTC - QUESTIONS SECTION

​Questions? +​1(855)595-2999

EverSmile® SQUIRT FOAMING MOUTHWASH - BUBBLE GUM Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

-------------------------------------

EverSmile​®

SQUIRT

   ​FOAMING

 MOUTHWASH

WITH FLUORIDE

Bubble gum

120 uses per bottles

 100 mL (3.38 fl oz)

Manufactured By

EverBrands, Inc

11791 Monarch St

Garden Grove,

CA 92841

(855)595-2999

info@eversmilewhite.com

eversmilewhite.com

squirt bubblegumsquirt bubblegum

RES

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
240698sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral RinsePSN1
240698sodium fluoride 0.5 MG/ML MouthwashSCD1
240698sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral RinseSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72655-702-01EverSmile Squirt100 mL in 1 BOTTLE, PUMPLIQUID1001

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72655-70272655-702-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
EverSmile SquirtSODIUM FLUORIDE 0.05%Everbrands, Inc.bc0ef174-2909-469a-b629-0eab4412bdfc2026-04-20WarningsExact identifier
ndc (package): 72655-702-01
ndc (product): 72655-702
ndc11 (package): 72655070201
spl id: 3bb09e05-affd-4102-a8b0-c37120d979ba
spl set id: bc0ef174-2909-469a-b629-0eab4412bdfc

Reported adverse events (FAERS/openFDA)#

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