FDA.reportPublic FDA data

Dry Eye Relief

Manufacturer
Similasan Corporation
Effective date
2021-02-15
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:19:19

Label at a glance#

ProductDry Eye Relief
Active ingredientATROPA BELLADONNA, EUPHRASIA STRICTA, MERCURIC CHLORIDE
Label structure10 sections

Indications and uses

According to homeopathic principles, the active ingredients in this product temporarily relieve minor symptoms such as: • dry eye • redness of eyes and lids • reflex watering secondary to dry eye

Dosage and administration

For adults and children age 2 and over: • remove tamper-evident seal from neck of bottle • twist cap off bottle • DON'T squeeze bottle, squeeze plastic tip to release 1 to 2 drops into eye • apply as needed • replace cap after use

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Belladonna† 6X

Euphrasia officinalis (Eyebright) 6X

Mercurius sublimatus 15X

Purpose

OTC - PURPOSE SECTION

dryness, redness

redness

dryness

Uses*

INDICATIONS & USAGE SECTION

According to homeopathic principles, the active ingredients in this product temporarily relieve minor symptoms such as:

• dry eye

• redness of eyes and lids

• reflex watering secondary to dry eye

Warnings

WARNINGS SECTION

• For external use only.

• According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms).

• Replace cap tightly after every use.

• To avoid contamination, do not touch the tip of the bottle to any surface.

• To avoid contamination use within 30 days of opening. Expiration date only refers to unopened bottle.

• Our drops will not harm contact lenses, however we recommend not wearing contacts while experiencing eye irritation.

If pregnant, trying to get pregnant or breast feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Do not use:

OTC - DO NOT USE SECTION

• if the solution changes color or becomes cloudy

Stop use and ask a doctor if:

OTC - STOP USE SECTION

• symptoms worsen or persist for more than 72 hours

• you experience eye pain or changes in vision

Directions

DOSAGE & ADMINISTRATION SECTION

For adults and children age 2 and over:

• remove tamper-evident seal from neck of bottle

• twist cap off bottle

• DON'T squeeze bottle, squeeze plastic tip to release 1 to 2 drops into eye

• apply as needed

• replace cap after use

Other Information

OTHER SAFETY INFORMATION

Active ingredients are manufactured according to homeopathic principles.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Borate buffer, Purified water, Silver sulfate (as preservative), Sodium nitrate

Questions?

OTC - QUESTIONS SECTION

Reach our representatives at 1-800-240-9780 or getinfo@similasanusa.com.

www.SimilasanUSA.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


Dry Eye
Relief
STERILE
EYE DROPS
10 ml/0.33 fl oz

Dry Eye Relief STERILE EYE DROPS 10 ml/0.33 fl ozDry Eye Relief STERILE EYE DROPS 10 ml/0.33 fl oz

Dry Eye Relief STERILE EYE DROPS 10 ml/0.33 fl ozDry Eye Relief STERILE EYE DROPS 10 ml/0.33 fl oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59262-374-112025-01-30C16284748780-1ba0f9c33-1adb-a910-e053-dadaa90a0b85Dry Eye Relief, 10ml
59262-374-112021-02-10C16284748780-1ba0f9c33-1adb-a910-e053-dadaa90a0b85Dry Eye Relief, 10ml
59262-374-112021-01-29C16284748780-1ba0f9c33-1adb-a910-e053-dadaa90a0b85Dry Eye Relief, 10ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59262-374-11Dry Eye Relief10 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS104
59262-374-11Dry Eye Relief1 in 1 CARTONSOLUTION/ DROPS14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59262-374DRY EYE RELIEF (ATROPA BELLADONNA, EUPHRASIA STRICTA AND MERCURIC CHLORIDE) SOLUTION/ DROPS [SIMILASAN CORPORATION]4Legacy NDC, 2 package rows20230106_b8eb74cf-9451-4305-a14a-3d0fc0b0c10d.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59262-37459262-374-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ATROPA BELLADONNAWQZ3G9PF0HACTIB
EUPHRASIA STRICTAC9642I91WLACTIB
MERCURIC CHLORIDE53GH7MZT1RACTIB
WATER059QF0KO0RIACT
SILVER SULFATE8QG6HV4ZPOIACT
SODIUM NITRATE8M4L3H2ZVZIACT

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
124b7379-b6b5-4b2b-8df2-06373ba8dd7fb8eb74cf-9451-4305-a14a-3d0fc0b0c10d2021-02-15WarningsExact identifier
spl id: 124b7379-b6b5-4b2b-8df2-06373ba8dd7f
spl set id: b8eb74cf-9451-4305-a14a-3d0fc0b0c10d

Reported adverse events (FAERS/openFDA)#

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