FDA.reportPublic FDA data

Natural Eyes Complete Eye Relief

Manufacturer
TRP Company
Effective date
2025-03-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:32:38

Label at a glance#

ProductNatural Eyes Complete Eye Relief Fast Dissolving Tables
Active ingredientLOESELIA MEXICANA WHOLE, SULFUR, RUTA GRAVEOLENS FLOWERING TOP, MERCURIC CHLORIDE, EUPHRASIA STRICTA
Label structure13 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Euphrasia officianalis 6X

Hoitzia 6X

Mercurius corrosivus 15X

Ruta graveolens 6X, 12X

Sulphur 9X, 15X

Purpose

OTC - PURPOSE SECTION

Euphrasia officianalis - Itchiness, grittiness

Hoitzia - Dryness, redness

Mercurius corrosivus HPUS 15X - Burning, swelling

Ruta graveolens - Tired eyes, eye strain

Sulphur HPUS - Redness, dryness

INDICATIONS & USAGE SECTION

Uses*
According to homeopathic indications these ingredients provide temporary relief from eye irritation after serious causes have been ruled out by a physician.

*These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS SECTION

Warnings:

A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES.

  • This product is intended to complement, not replace, standard medical treatment.
  • Initial worsening of symptoms may occur.
  • This product is intended to be taken orally. Do not use in eyes or nose.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNINGS SECTION

  • In case of overdose, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if:

• You experience eye pain or change in vision, continued redness, or irritation of the eye. • The condition worsens.
• Symptoms last longer than 72 hours.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Suitable for adults and children ages 5 and over.
  • Dissolve entire tablet under tongue.
  • Do not chew or swallow whole.
  • Take 1 tablet 3 times a day or as directed by a physician.
  • Use up to 6 times a day as needed.
  • Take at least 10 minutes before or at least 10 minutes after eating or drinking.
  • Children under the age of 5: Consult a physician before use.

SPL UNCLASSIFIED SECTION

Other information

  • Homeopathic remedies may not be effective for everyone.
  • Individual results may vary.
  • Complete Eye Relief Fast Dissolving Tablets TM are homeopathic dilutions, for details see www.thereliefproducts.com

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients
Black carrot extract (colorant), Croscarmellose sodium, Lactose, Magnesium stearate, Maltodextrin, Microcrystalline cellulose, Sucrose.

Do not use if:

OTC - DO NOT USE SECTION

Do not use if:

• You frequently contract infections that do not clear up easily. • You experience eye pain or changes in vision.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCarton

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17312-422-14Natural Eyes Complete Eye ReliefFast Dissolving Tables2 in 1 PACKAGETABLET, ORALLY DISINTEGRATING21
17312-422-14Natural Eyes Complete Eye ReliefFast Dissolving Tables24 in 1 BLISTER PACKTABLET, ORALLY DISINTEGRATING241

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17312-422NATURAL EYES COMPLETE EYE RELIEF FAST DISSOLVING TABLES (EUPHRASIA OFFICIANALIS, HOITZIA, MERCURIUS CORROSIVUS, RUTA GRAVEOLENS, SULPHUR) TABLET, ORALLY DISINTEGRATING [TRP COMPANY]1Current NDC, 2 package rows20250321_30a1d9aa-3966-0b91-e063-6294a90ae72b.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
17312-42217312-422-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
LOESELIA MEXICANA WHOLEXA8YCV5M3EACTIB
SUCROSEC151H8M554IACT
BLACK CARROT27793ZFD2LIACT
CROSCARMELLOSE SODIUMM28OL1HH48IACT
LACTOSEJ2B2A4N98GIACT
CELLULOSE, MICROCRYSTALLINEOP1R32D61UIACT
MALTODEXTRIN7CVR7L4A2DIACT
MAGNESIUM STEARATE70097M6I30IACT
SULFUR70FD1KFU70ACTIB
RUTA GRAVEOLENS FLOWERING TOPN94C2U587SACTIB
MERCURIC CHLORIDE53GH7MZT1RACTIB
EUPHRASIA STRICTAC9642I91WLACTIB

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
Natural Eyes Complete Eye Relief Fast Dissolving TablesEUPHRASIA OFFICIANALIS, HOITZIA, MERCURIUS CORROSIVUS, RUTA GRAVEOLENS, SULPHURTRP Company30a1d9aa-3966-0b91-e063-6294a90ae72b2025-03-18WarningsExact identifier
ndc (package): 17312-422-14
ndc (product): 17312-422
ndc11 (package): 17312042214
spl id: 30a1e23f-5af9-06a6-e063-6294a90ace41
spl set id: 30a1d9aa-3966-0b91-e063-6294a90ae72b

Reported adverse events (FAERS/openFDA)#

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