LACRIFRESH HYDRAPF

Manufacturer
AVIZOR, S.A.
Effective date
2025-10-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:41:47

Label at a glance#

ProductLACRIFRESH HYDRAPF
Active ingredientPOVIDONE, GLYCERIN
Label structure9 sections

Dosage and administration

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

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTSPURPOSES
Glycerin 0.63%Lubricant
Povidone 0.25%Lubricant

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

  • 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 SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use

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

OTC - WHEN USING SECTION

When using this product

  • Do not touch tip of container to any surface to avoid contamination
  • Replace cap after using

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

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

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

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

Other information

OTHER SAFETY INFORMATION

Other information

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

INACTIVE INGREDIENT SECTION

Inactive ingredients

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

Questions or comments?

OTC - QUESTIONS SECTION

Questions or comments?

Call 1-800-714-1824

PACKAGE LABEL.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)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagePackage

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2625120glycerin 0.63 % / povidone 0.25 % Ophthalmic SolutionPSN1
2625120glycerin 6.3 MG/ML / povidone 2.5 MG/ML Ophthalmic SolutionSCD1
2625120glycerin 0.63 % / povidone 0.25 % Ophthalmic SolutionSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130382808000025GTIN-13: 0382808000025
EAN-13: 0382808000025
GTIN-12: 382808000025
UPC-A: 382808000025
GTIN storage (14 digits): 00382808000025
LACRIFRESH HYDRAPF USA.jpg
Data codeData MatrixEST5027FLACRIFRESH HYDRAPF USA.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82808-004-01LACRIFRESH HYDRAPF1 in 1 CASESOLUTION/ DROPS11
82808-004-01LACRIFRESH HYDRAPF10 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS101

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82808-00482808-004-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LACRIFRESH HYDRAPFGLYCERIN, POVIDONEAVIZOR, S.A.41bbd23e-0ec8-eb18-e063-6294a90a46d12025-10-27WarningsExact identifier
ndc (package): 82808-004-01
ndc (product): 82808-004
ndc11 (package): 82808000401
spl id: 41bbd23e-0ec9-eb18-e063-6294a90a46d1
spl set id: 41bbd23e-0ec8-eb18-e063-6294a90a46d1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.