Natural Eyes Complete Eye Relief

Product NDC
17312-422
11-digit product format
173120422
Labeler code
17312
Product ID
17312-422_30a1e23f-5af9-06a6-e063-6294a90ace41
Type
HUMAN OTC DRUG
Nonproprietary name
Euphrasia officianalis, Hoitzia, Mercurius corrosivus, Ruta graveolens, Sulphur
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Labeler
TRP Company
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2025-03-16
Substance
EUPHRASIA STRICTA; LOESELIA MEXICANA WHOLE; MERCURIC CHLORIDE; RUTA GRAVEOLENS FLOWERING TOP; SULFUR
Active strength
6; 6; 15; 6; 9 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Natural Eyes Complete Eye Relief
Brand name suffix
Fast Dissolving Tables
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LOESELIA MEXICANA WHOLE6 [hp_X]/1
SULFUR6 [hp_X]/1
RUTA GRAVEOLENS FLOWERING TOP15 [hp_X]/1
MERCURIC CHLORIDE6 [hp_X]/1
EUPHRASIA STRICTA9 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
XA8YCV5M3EInternal UNII lookup
70FD1KFU70Internal UNII lookup
N94C2U587SInternal UNII lookup
53GH7MZT1RInternal UNII lookup
C9642I91WLInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
30a1d9aa-3966-0b91-e063-6294a90ae72bAvailable on FDA.report

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

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 (product): 17312-422

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
17312-422-14173120422142 BLISTER PACK in 1 PACKAGE (17312-422-14) / 24 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK2 blister pack2025-03-17NoNoCurrent