Cataract

Manufacturer
Natural Ophthalmics, Inc
Effective date
2023-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:25:18

Label at a glance#

ProductCataract
Active ingredientSILICON DIOXIDE, EUPHRASIA STRICTA, CALCIUM FLUORIDE, JACOBAEA MARITIMA WHOLE, SEPIA OFFICINALIS JUICE, TRIBASIC CALCIUM PHOSPHATE, CAUSTICUM
Label structure9 sections

Dosage and administration

Dissolve three pellets under tongue three times per day or as directed by a medical professional.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Calc fluor 12X; Calc phos 12X; Causticum 7X; Cineraria maritima 6X; Euphrasia 7X; Sepia 7X; Silicea 13X

INDICATIONS & USAGE SECTION

According to homeopathic indications, these ingredients are intended to stimulate and help the body counteract the symptoms of cataracts.

Warnings:

WARNINGS SECTION

• For oral use only. If you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours, discontinue use and consult a physician.

OTC - PREGNANCY OR BREAST FEEDING SECTION

Pregnant or nursing women should consult their doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INACTIVE INGREDIENT SECTION

organic sucrose

Directions:

DOSAGE & ADMINISTRATION SECTION

Dissolve three pellets under tongue three times per day or as directed by a medical professional.

SPL UNCLASSIFIED SECTION

Do not use if tamper evident seal is broken.

*The letters “HPUS” indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

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

Manufactured for: Natural Ophthalmics, Inc. PO Box 1510 Dillon, CO 80435 PH: 877-220-9710

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68770-210-42Cataract600 in 1 TUBEPELLET6002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68770-210CATARACT (CALCIUM FLUORIDE, TRIBASIC CALCIUM PHOSPHATE, CAUSTICUM, JACOBAEA MARITIMA WHOLE, EUPHRASIA STRICTA, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE) PELLET [NATURAL OPHTHALMICS, INC]2Legacy NDC, 1 package rows20240101_ddab7487-cd46-5597-e053-2a95a90a7a35.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68770-21068770-210-42

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
0dd79dde-3e32-6073-e063-6294a90a0f06ddab7487-cd46-5597-e053-2a95a90a7a352023-12-31WarningsExact identifier
spl id: 0dd79dde-3e32-6073-e063-6294a90a0f06
spl set id: ddab7487-cd46-5597-e053-2a95a90a7a35

Reported adverse events (FAERS/openFDA)#

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