Pink Eye Relief

Manufacturer
Similasan Corporation
Effective date
2021-10-06
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:19:13

Label at a glance#

ProductPink Eye Relief
Active ingredientATROPA BELLADONNA, EUPHRASIA STRICTA, CALCIUM SULFIDE
Label structure14 sections

Indications and uses

According to homeopathic principles, the active ingredients in this product temporarily relieve minor eye symptoms: • excessive watery (clear) discharge • sensation of grittiness • redness and burning

Dosage and administration

For adults and children ages 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†

†containing 0.000002% alkaloids calculated as hyoscyamine

Purpose

OTC - PURPOSE SECTION

dryness, redness, burning, sensation of grittiness

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Euphrasia officinalis (Eyebright) 6X

Purpose

OTC - PURPOSE SECTION

watery discharge

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Hepar sulphuris 12X

Purpose

OTC - PURPOSE SECTION

redness, stinging

Uses*

INDICATIONS & USAGE SECTION

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

• excessive watery (clear) discharge

• sensation of grittiness

• redness and burning

Warnings

WARNINGS SECTION

• For external use only.

• Children under 2 years of age should be seen by a physician.

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

• 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.

• Replace cap tightly after every use.

• ‡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

• you experience eye pain or changes in vision

• symptoms worsen or persist for more than 72 hours

• you might have a serious underlying medical cause for an infection

Directions

DOSAGE & ADMINISTRATION SECTION

For adults and children ages 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

For your protection do not use if tamper evident seal around neck of bottle is missing or broken.

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 59262-365-11
Similasan
Pink eye
Relief
10 mL/ 0.33 fl oz

NDC 59262-365-11 Similasan Pink eye Relief 10 mL/ 0.33 fl ozNDC 59262-365-11 Similasan Pink eye Relief 10 mL/ 0.33 fl oz

NDC 59262-365-11 Similasan Pink eye Relief 10 mL/ 0.33 fl ozNDC 59262-365-11 Similasan Pink eye Relief 10 mL/ 0.33 fl oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59262-365-112025-01-30C16284748780-19d75b9d0-f4de-f424-e053-dadaa90a57cePink Eye Relief 10ml
59262-365-112020-09-28C16284748780-19d75b9d0-f4de-f424-e053-dadaa90a57cePink Eye Relief 10ml
59262-365-112020-01-31C16284748780-19d75b9d0-f4de-f424-e053-dadaa90a57cePink Eye Relief 10ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59262-365-11Pink Eye Relief10 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS104

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59262-365PINK EYE RELIEF (BELLADONNA, EUPHRASIA OFFICINALIS, HEPAR SULPHURIS) SOLUTION/ DROPS [SIMILASAN CORPORATION]4Legacy NDC, 1 package rows20230106_652b49f6-3eb9-4ad4-b0a5-de4f64df30df.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
59262-36559262-365-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
60c1a687-1e43-4007-9eae-cc616f111d0e652b49f6-3eb9-4ad4-b0a5-de4f64df30df2021-10-06WarningsExact identifier
spl id: 60c1a687-1e43-4007-9eae-cc616f111d0e
spl set id: 652b49f6-3eb9-4ad4-b0a5-de4f64df30df

Reported adverse events (FAERS/openFDA)#

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