CVS EYEWASH- purified water kit

CVS Eyewash by

Drug Labeling and Warnings

CVS Eyewash by is a Otc medication manufactured, distributed, or labeled by CVS, Tender Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Purified Water USP 98.577% w/v

Purpose

Eyewash

Use

Use for flushing the eye to remove loose foreign material

Warnings

To avoid contamination, do not touch tip of container to any surface.

Do not reuse.

Once opened, discard.

If you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists, consult a doctor.

Obtain immediate medical treatment for all open wounds in or near the eyes.

If solution changes color or becomes cloudy do not use nor, if twist-off Tamper Evident top is broken or missing.

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.

Inactive Ingredients

Disodium EDTA

Polyhexanide

Sodium Chloride

Sodium Hydroxide

Sodium Phosphate, Dibasic

Sodium Phosphate, Monobasic

Storage and Handling

Store 36°F-104°F

Use 59°F-86°F

Packaging

INGREDIENTS AND APPEARANCE

CVS EYEWASH 
purified water kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-209

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-209-12	5 in 1 BOX	10/09/2017
1	NDC: 69842-209-10	1 in 1 VIAL; Type 0: Not a Combination Product

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 VIAL	15 mL

Part 1 of 1

A-MED BRAND FIRST AID EYE AND SKIN-RINSE 
purified water solution

Product Information
Item Code (Source)	NDC: 59276-209
Route of Administration	CUTANEOUS, OPHTHALMIC, TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	98.577 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM PHOSPHATE, DIBASIC DODECAHYDRATE (UNII: E1W4N241FO)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
POLIHEXANIDE (UNII: 322U039GMF)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59276-209-10	15 mL in 1 VIAL; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	11/01/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	10/09/2017

Labeler - CVS (062312574)

Establishment
Name	Address	ID/FEI	Business Operations
Tender Corporation		064437304	manufacture(69842-209)