Plum Duo Emergency Eyewash description, usages, side effects, indications, overdosage, supplying and lots more!

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Plum Duo Emergency Eyewash

Bel-Art Products

Plum Emergency Eyewash Duo


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Purified water 99.1%

Purpose

Emergency eyewash and skin flush

Plum Duo Emergency Eyewash Uses

For flushing the eye and skin to reduce chances of severe injury caused by acid, alkali, or particulate contamination.

Warnings

Do not use


● for injection  ● in intraocular surgery  ● internally


When using this product

● avoid contamination  ● do not reuse

Once opened, discard.

Ask doctor if you have

● eye pain  ● changes in vision

● redness or irritation of the eye after use  ● an injury caused by alkali

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

● do not dilute solution or reuse bottle

● to open, twist cap in the direction of the arrow

● center the DUO between the eyes to simultaneously wash both eyes

● control flow of solution by pressure on bottle   ● flush affected area as needed

● continue to flush with water as necessary   ● obtain medical treatment

Plum Duo Emergency Eyewash Other information


● not for use as a contact lens solution  ● twist cap to open

● use before expiration date marked on bottle

● store at room temperature 5° to 35° C (41° to 95°F)

Inactive ingredient

Sterile sodium chloride

Questions or Comments?

Call toll-free number 1-800-423-5278

Distributed by

Bel-Art Products ● 661 Route 23 South ● Wayne, NJ 07470

Plum

EMERGENCY EYEWASH

NCD 67691-101-11

DUO

STERILE

1000 ml (33.8 fl oz)

Bel-Art Products
661 Route 23 South, New Jersey, 07470
Tel: 973-694-0500  ● Fax: 973-694-7199  ● www.belart.com

Compliance: ANSI/ISEA Z358.1-2009
(As Personal Eyewash Only)

Duo Saline Label.jpg


Plum Duo Emergency Eyewash

Plum Duo Emergency Eyewash

Water LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:67691-101
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
water 99.1 mL

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:67691-101-11 1000 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2010-06-23


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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