EyeClear Pro

Manufacturer
Silver Star Brands | Vitality Works
Effective date
2019-02-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:11:01

Label at a glance#

ProductEyeClear Pro
Active ingredientCAUSTICUM, EUPHRASIA STRICTA, NAPHTHALENE, QUASSIA AMARA WOOD, JACOBAEA MARITIMA, SILICON DIOXIDE, PHOSPHORUS, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CALCIUM FLUORIDE, SODIUM CHLORIDE
Label structure10 sections

Indications and uses

Uses*: For temporary relief of symptoms of common eye irritations: mineral accumulations, tearing, light sensitivity, eye fatigue, redness, itching. *This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Dosage and administration

Directions: Mix in 1/4 cup of water and sip slowly. If preferred, drops may be taken directly into the mouth. Adults: Take 0.50 mL. Children 2-12: Take 0.25 mL. Repeat 3 times daily as needed or until symptoms subside.

Label contents#

Full prescribing information#

HPUS Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

HPUS Active Ingredients: Equal volumes of each ingredient in 10X, 30X, 1LM potencies: Calc carb, Calc fluor, Causticum, Cineraria, Euphrasia, Naphthalinum, Nat mur, Phos, Quassia, Silicea.

The letters HPUS indicate that the components in this product are offically monographed in the Homeopathic Pharmacopoeia of the United States.

Uses*

INDICATIONS & USAGE SECTION

Uses*: For temporary relief of symptoms of common eye irritations: mineral accumulations, tearing, light sensitivity, eye fatigue, redness, itching.

*This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Warnings

WARNINGS SECTION

Warnings: If symptoms persist or worsen, consult a healthcare professional. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: Mix in 1/4 cup of water and sip slowly. If preferred, drops may be taken directly into the mouth. Adults: Take 0.50 mL. Children 2-12: Take 0.25 mL. Repeat 3 times daily as needed or until symptoms subside.

OTHER SAFETY INFORMATION

Contains no artificial flavors or colorants. No gluten added.

Tamper resistant for your protection. Use only if safety seal is intact.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Inactive Ingredients: USP purified water, vegetable glycerin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medication out of reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a healthcare professional before use.

OTC - PURPOSE SECTION

Relieves symptoms of mineral buildup & eye irritation.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EyeClear ProEyeClear Pro

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
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e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
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
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
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ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68703-321-022021-01-29C16284748780-1ba0f9c33-394e-a910-e053-dadaa90a0b85NativeRemedies® EyeClear Pro™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68703-321-02EyeClear Pro59 mL in 1 BOTTLE, GLASSLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68703-321EYECLEAR PRO (CALC CARB, CALC FLUOR, CAUSTICUM,CINERARIA, EUPHRASIA, NAPHTHALINUM, NAT MUR, PHOS, QUASSIA, SILICEA) LIQUID [SILVER STAR BRANDS]1Legacy NDC, 1 package rows20190304_824147d2-c832-217d-e053-2991aa0ae3ba.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68703-32168703-321-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
824147d2-c833-217d-e053-2991aa0ae3ba824147d2-c832-217d-e053-2991aa0ae3ba2019-02-19WarningsExact identifier
spl id: 824147d2-c833-217d-e053-2991aa0ae3ba
spl set id: 824147d2-c832-217d-e053-2991aa0ae3ba

Reported adverse events (FAERS/openFDA)#

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