REAL EYEWASH- purified water solution

Real Eyewash by

Drug Labeling and Warnings

Real Eyewash by is a Otc medication manufactured, distributed, or labeled by Oliver Landon Intl Inc.. 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

For external use only

• 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.

Other information

• Store at 36° - 104°F
• Use at 59° - 86°F
• Keep out of direct sunlight

Inactive ingredients

Disodium EDTA

Polyhexanide

Sodium Chloride

Sodium Hydroxide

Sodium Phosphate, Dibasic dodecahydrate

Sodium Phosphate, Monobasic dihydrate

SPL UNCLASSIFIED SECTION

Manufactured in Singapore

Oliver Landon Intl Inc.

The Grove 21 Pine Road
Belleville, St. Michael,
BB 11113
Barbados © 2018

All Rights Reserved.

info@OliverLandon.biz

Package/Label Principal Display Panel – Real Eye Wash

INGREDIENTS AND APPEARANCE

REAL EYEWASH 
purified water solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59276-208
Route of Administration	OPHTHALMIC

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59276-208-12	5 in 1 BOX	04/13/2018
1	NDC: 59276-208-10	15 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2	NDC: 59276-208-14	10 in 1 BOX	04/13/2018
2	NDC: 59276-208-10	15 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
3	NDC: 59276-208-16	30 in 1 BOX	04/13/2018
3	NDC: 59276-208-10	15 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
4	NDC: 59276-208-18	60 in 1 BOX	04/13/2018
4	NDC: 59276-208-10	15 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
5	NDC: 59276-208-21	4 in 1 BOX	04/13/2018
5	NDC: 59276-208-20	30 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
6	NDC: 59276-208-31	1 in 1 BOX	04/13/2018
6	NDC: 59276-208-30	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
7	NDC: 59276-208-41	1 in 1 BOX	04/13/2018
7	NDC: 59276-208-40	118 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
8	NDC: 59276-208-51	1 in 1 BOX	04/13/2018
8	NDC: 59276-208-50	148 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
9	NDC: 59276-208-61	1 in 1 BOX	04/13/2018
9	NDC: 59276-208-60	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
10	NDC: 59276-208-71	1 in 1 BOX	04/13/2018
10	NDC: 59276-208-70	350 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
11	NDC: 59276-208-81	1 in 1 BOX	04/13/2018
11	NDC: 59276-208-80	474 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
12	NDC: 59276-208-82	2 in 1 BOX	04/13/2018
12	NDC: 59276-208-80	474 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
13	NDC: 59276-208-91	1 in 1 BOX	04/13/2018
13	NDC: 59276-208-90	947 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
14	NDC: 59276-208-92	2 in 1 BOX	04/13/2018
14	NDC: 59276-208-90	947 mL in 1 BOTTLE, PLASTIC; 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	04/13/2018

Labeler - Oliver Landon Intl Inc. (815240195)