LACRIFRESH HYDRAPF- glycerin, povidone solution/ drops

LACRIFRESH HYDRAPF by

Drug Labeling and Warnings

LACRIFRESH HYDRAPF by is a Otc medication manufactured, distributed, or labeled by AVIZOR, S.A.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

• ACTIVE INGREDIENTS: PURPOSES
• Glycerin 0.63%: Lubricant
• Povidone 0.25%: Lubricant

INDICATIONS & USAGE

• 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 relief dryness of the eye

WARNINGS

For external use only

Do not use

• If solution changes color or becomes cloudy
• If you are sensitive to any ingredient in this product

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 children

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

Directions

Directions

• Instill 1 or 2 drops in the affected eye(s) as needed

Other information

Other information

• Store at 15º-30ºC (59º-86ºF)
• Discard the product within 90 days of first opening

INACTIVE INGREDIENT

Inactive ingredients

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

Questions or comments?

Questions or comments?

Call 1-800-714-1824

PRINCIPAL DISPLAY PANEL

AVIZOR

Lacrifresh

LUBRICANT EYE DROPS

PRESERVATIVE FREE

HydraPF

Dry Eye Relief

Instant Comfort and Hydration

Protects and Lubricates the Eye Surface

Enhanced with

0.63% Glycerin + 0.25% Povidone

Sterile

0.33 FL OZ (10 mL)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LACRIFRESH HYDRAPF 
glycerin, povidone solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82808-004
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE (UNII: FZ989GH94E) (POVIDONE - 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
SODIUM BORATE (UNII: 91MBZ8H3QO)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
BORIC ACID (UNII: R57ZHV85D4)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82808-004-01	1 in 1 CASE	11/03/2025
1		10 mL in 1 BOTTLE, DROPPER; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	11/03/2025

Labeler - AVIZOR, S.A. (465588731)

Registrant - AVIZOR, S.A. (465588731)

Establishment
Name	Address	ID/FEI	Business Operations
AVIZOR, S.A.		465588731	manufacture(82808-004) , label(82808-004) , pack(82808-004)