EYE LOVE HEYEDRATE LONG LASTING HYDRATION- glycerin, povidone solution/ drops

Eye Love Heyedrate Long Lasting Hydration by

Drug Labeling and Warnings

Eye Love Heyedrate Long Lasting Hydration by is a Otc medication manufactured, distributed, or labeled by Physician Recommended Neutraceuticals, L.P., KC Pharmaceuticals, Inc., Avizor, S. A.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Glycerin 0.63%

Povidone 0.25%

Purpose

Lubricant

Lubricant

Uses

• for the temporary relief of burning and irritation due to dryness of the eye
• for the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun
• for use as a protectant against further irritation or to relieve dryness of the eye

Warnings

For external use only

Do not use

• if solution changes color or becomes cloudy
• if tamper evident ring is broken or missing

When using this product

• do not touch tip of container to any surface to avoid contamination
• replace cap after using

Stop use and ask a doctor if

• you experience eye pain, changes in vision, continued redness or irritation of the eye
• condition worsens or persists for more than 72 hours

Keep out of reach of childeren.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

• remove tamper evident ring, then remove cap
• tip bottle at a downward angle or upside down (to deliver drop to eye)
• squeeze bottle to instill 1 or 2 drops in the affected eye(s) as needed
• replace cap after use

Other information

store at 15°-30°C (59°-86°F)

Inactive ingredients

boric acid, calcium chloride, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, sodium hyaluronate

Questions or comments?

Call-1-888-EYE-LUV9

Monday-Friday

Eye Love Heyedrate Lubricant Eye Drops 10mL

INGREDIENTS AND APPEARANCE

EYE LOVE HEYEDRATE LONG LASTING HYDRATION 
glycerin, povidone solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83201-002
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE (UNII: FZ989GH94E) (POVIDONE, UNSPECIFIED - UNII:FZ989GH94E)	POVIDONE	0.25 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	0.63 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM BORATE (UNII: 91MBZ8H3QO)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83201-002-10	1 in 1 BOX	02/08/2023
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	02/08/2023

Labeler - Physician Recommended Neutraceuticals, L.P. (018807840)

Registrant - KC Pharmaceuticals, Inc. (174450460)

Establishment
Name	Address	ID/FEI	Business Operations
KC Pharmaceuticals, Inc.		174450460	pack(83201-002) , label(83201-002)

Establishment
Name	Address	ID/FEI	Business Operations
Avizor, S. A.		465588731	manufacture(83201-002)