REFILL BUNDLE 8 LARGE OFFICE- water kit

Refill Bundle 8 Large Office by

Drug Labeling and Warnings

Refill Bundle 8 Large Office by is a Otc medication manufactured, distributed, or labeled by CMC Group, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Eyewash 1 oz - 49687-0010 DRUG FACTS

Active ingredient

Purified Water 99.1%

Purpose

Eyewash

Use

For cleansing the eye to help relieve irritation or burning by removing loose foreign material

Warnings

For external use only.

Do not use

if solution changes color or becomes cloudy

When using this product

to avoid contamination, do not touch tip of container to any surface do not reuse once opened, discard obtain immediate medical treatment for all open wounds in or near the eyes

Stop use and ask a doctor if

you experience: eye pain changes in vision continued redness irritation of the eye condition worsens or persists

Keep out of reach of children.

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

Directions

Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle

Other information

not for use as contact lens solution

use before expiration date marked on the bottle

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

Inactive ingredients

Benzalkonium chloride, sodium chloride

Package Labeling:

Package Labeling:

INGREDIENTS AND APPEARANCE

REFILL BUNDLE 8 LARGE OFFICE 
water kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49687-0030

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49687-0030-0	1 in 1 KIT	02/13/2018

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 TUBE	30 mL

Part 1 of 1

EYE WASH 
water solution

Product Information
Item Code (Source)	NDC: 49687-0010
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	991 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49687-0010-0	4 in 1 KIT
1		30 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part349	02/13/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	02/13/2018

Labeler - CMC Group, Inc. (005583328)