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#
Contacts and useful links#
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
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
res
Products#
Every source-derived product name is available through these pages.
- Preop Rinse
- HYDROGEN PEROXIDE
- WATER
- GLYCERIN
- POVIDONE K30
- POLYETHYLENE GLYCOL 8000
- SODIUM LAURYL SULFATE
- SUCRALOSE
- SODIUM CITRATE
- SODIUM BENZOATE
- ETIDRONIC ACID
- MENTHA ARVENSIS LEAF OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72655-100 | 72655-100-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HYDROGEN PEROXIDE | BBX060AN9V | ACTIB |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| POVIDONE K30 | U725QWY32X | IACT |
| POLYETHYLENE GLYCOL 8000 | Q662QK8M3B | IACT |
| SODIUM LAURYL SULFATE | 368GB5141J | IACT |
| SUCRALOSE | 96K6UQ3ZD4 | IACT |
| SODIUM CITRATE | 1Q73Q2JULR | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| ETIDRONIC ACID | M2F465ROXU | IACT |
| MENTHA ARVENSIS LEAF OIL | 1AEY1M553N | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 28560376-4bc9-4f6d-b306-483eb1465355 | c14f8518-3642-4bb7-8d59-7aa664e2a381 | 2021-03-19 | Warnings | c14f8518-3642-4bb7-8d59-7aa664e2a381 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
