Preop Rinse

Manufacturer
Everbrands, Inc. dba EverPure, Inc.
Effective date
2020-12-30
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:58:05

Label at a glance#

ProductPreop Rinse
Active ingredientHYDROGEN PEROXIDE
Label structure5 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

PREOP™ RINSE
PRE TREATMENT
FOAMING RINSE

INSTRUCTIONS FOR USE SECTION

Instructions For Use
Prior to commencing dental procedures, dispense 2 pumps (4-5 ml)
of PreOp™ Rinse into a disposable paper cup and have patient rinse
and swish for 15 seconds. Optional: Seat patient in chair, have
patient rinse, and then instead of expectorating, use saliva ejector
to prevent sink contamination. After use, rinsing with water is
optional. For extended procedures, have patient rinse again.

SPL UNCLASSIFIED SECTION

Ingredients
Water, hydrogen peroxide, glycerine, PVP PEG, sodium lauryl
sulfate, sucralose, sodium citrate, sodium benzoate, etidronic acid,
organic mint oil or bubble gum flavor (based on front label).

WARNINGS AND PRECAUTIONS SECTION

Warnings/Precautions
If irritation (such as redness, swelling, soreness) of the gums or
mouth occurs, discontinue use & consult your dentist. Adult
supervision is required for use by children under 12. Avoid contact
with eyes, skin, or hair; flush with water if contact is made. Avoid
swallowing; do not induce vomiting. Do not apply directly to gums
or under tongue. Do not use if nursing or pregnant. Keep away
from sunlight & heat as contents may pressurize. Use of this
product is not intended to cure any disease. Not for systemic use.

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PREOP™ RINSE
PRE TREATMENT
FOAMING RINSE

SURFACTANT ENHANCED™

HYDROGEN PEROXIDE

Rx Only

475ml 16fl oz

Manufactured by EverBrands, Inc.
401 N. Oak St., Inglewood, CA 90302
eversmilewhite.com/preop
(855) 595-2999

72655-10072655-100

res

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72655-10072655-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
28560376-4bc9-4f6d-b306-483eb1465355c14f8518-3642-4bb7-8d59-7aa664e2a3812021-03-19WarningsExact identifier
spl set id: c14f8518-3642-4bb7-8d59-7aa664e2a381

Reported adverse events (FAERS/openFDA)#

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