Cataract Crystalline Lens

Manufacturer
Natural Ophthalmics, Inc
Effective date
2020-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:13:16

Label at a glance#

ProductCataract Crystalline Lens
Active ingredientJACOBAEA MARITIMA, EUPHRASIA STRICTA, CAUSTICUM, TRIBASIC CALCIUM PHOSPHATE, SEPIA OFFICINALIS JUICE, CALCIUM FLUORIDE, SILICON DIOXIDE
Label structure13 sections

Indications and uses

According to homeopathic principles these drops are indicated for the treatment of the symptoms of Cataract.* *Claims are based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

Instill 1drop in each eye three times per day or as directed by your doctor.

Storage and handling

Safe Storage Room temperature 59 o to 86 o (15 o to 30 o C)

Label contents#

Full prescribing information#

Homeopathic Purpose

OTC - PURPOSE SECTION

Cineraria Maritima HPUS6XIncreases circulation in the intraocular tissues
Euphrasia (Eyebright) HPUS6XGeneral dryness, redness and irritation of the eye and lids
Causticum HPUS8XEye pain
Calcarea phosphorica HPUS11XBlurry vision, eye pain from reading
Sepia HPUS8XGlares, black spots, veils, points, sparks, flashes and streaks of light
Calcarea fluorica HPUS11XCataract, corneal opacities, keratitis, flickering and floaters
Silicea HPUS11XSpotted vision, cataract, opacities, keratitis

*Claims are based on traditional homeopathic practice, not accepted medicalevidence. Not FDA evaluated

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Cineraria Maritima HPUS6X
Euphrasia (Eyebright) HPUS6X
Causticum HPUS8X
Calcarea phosphorica HPUS11X
Sepia HPUS8X
Calcarea fluorica HPUS11X
Silicea HPUS11X

"HPUS" indicates the active ingredients of this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified water
Sodium chloride
Sodium citrate
Polysorbate 80
Citric acid

Uses

INDICATIONS & USAGE SECTION

According to homeopathic principles these drops are indicated for the treatment of the symptoms of Cataract.*

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

Directions

DOSAGE & ADMINISTRATION SECTION

Instill 1drop in each eye three times per day or as directed by your doctor.

Warnings

WARNINGS SECTION

- For ophthalmic use.

For professional use only.

Do not use if tamper evident seal is torn, broken. or missing.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

If pregnant or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast feeding, ask a health professional before use.

Stop use and ask a doctor if:

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. The condition worsens. Symptoms last longer than 72 hours.

Do not use

OTC - DO NOT USE SECTION

Do not use if solution becomes cloudy.

Storage

STORAGE AND HANDLING SECTION

  • Safe Storage

Room temperature
59 o to 86 o (15 o to 30 o C)

OTC - QUESTIONS SECTION

Natural Ophthalmics, Inc
Dillon, CO, 80435
1-877-220-9710
www.natoph.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCarton

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68770-135-102022-01-28C16284748780-1d6a99b39-4299-a426-e053-dadaa90af4c2Cataract Crystalline Lens

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68770-135-10Cataract Crystalline Lens10 mL in 1 BOTTLE, DROPPERLIQUID101
68770-135-10Cataract Crystalline Lens1 in 1 PACKAGELIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68770-135CATARACT CRYSTALLINE LENS (CINERARIA MARITIMA, EUPHRASIA STRICTICA, CAUSTICUM, CALCAREA PHOSPHORICA, SEPIA, CALCAREA FLOURICA, SILICEA) LIQUID [NATURAL OPHTHALMICS, INC]1Legacy NDC, 2 package rows20200715_aa688936-d164-8326-e053-2995a90a0e6e.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68770-13568770-135-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
aa686dba-5f51-e08c-e053-2995a90a4a04aa688936-d164-8326-e053-2995a90a0e6e2020-07-14WarningsExact identifier
spl id: aa686dba-5f51-e08c-e053-2995a90a4a04
spl set id: aa688936-d164-8326-e053-2995a90a0e6e

Reported adverse events (FAERS/openFDA)#

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