Floaters Relief

Manufacturer
TRP Company
Effective date
2022-08-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:55:42

Label at a glance#

ProductFloaters Relief
Active ingredientSILICON DIOXIDE, SEPIA OFFICINALIS JUICE, CHELIDONIUM MAJUS, PHOSPHORUS, SODIUM CHLORIDE, POTASSIUM SULFATE, EUPHRASIA STRICTA, PHYSOSTIGMA VENENOSUM SEED
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsPurpose
Chelidonium HPUS 6xFloaters obstructing vision
Physostigma HPUS 12xShapes in vision
Euphrasia HPUS 6xIrritation
Kali Sulph. HPUS 10xSquiggly lines in vision
Natrium muriaticum HPUS 10xFloaters in vision
Phosphorus HPUS 12xDark dots in vision
Silicea HPUS 12xBlurry vision
Sepia HPUS 7xDust particles

"HPUS" indicates the active ingredients are in the Homeopathic Pharmacopoeia of the United States.

INDICATIONS & USAGE SECTION

Uses:*
According to homeopathic indications these ingredients provide temporary relief from symptoms such as:

• Floaters • Squiggly lines in vision • Irritation • Dark dots in vision • Shapes in vision • Dust particles in vision; 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.

For External Use Only.

  • This product is intended to complement not replace, standard medical treatment.
  • Initial worsening of symptoms may occur.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

WARNINGS SECTION

  • Contact lens wearers consult physician before use.
  • To avoid contamination - do not touch tip to any surface.
  • Replace cap after every use.
  • Use within 30 days of opening.
  • EXPIRATION DATE ONLY REFERS TO THE UNOPENED BOTTLE.
  • The use of this container by more than one person may spread infection.

Do not use:

OTC - DO NOT USE SECTION

  • If solution changes color or becomes cloudy.
  • If you frequently contract infections that do not clear up easily.
  • If you experience eye pain or changes in vision.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

  • You experience eye pain or change in vision, continued shapes, or floaters in vision.
  • The condition worsens.
  • Symptoms last longer than 72 hours.

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.

DOSAGE & ADMINISTRATION SECTION

Directions:

• Suitable for adults and children ages 2 and over. Children under the age of 2: Consult a physician before use. Squeeze 1-3 drops in the eye. Use several times per day as needed. Homeopathic remedies may not be effective for everyone. Individual results may vary.

SPL UNCLASSIFIED SECTION

Other information:

  • Non-prescription drug products cannot treat infections.
  • Store at room temperature 15° to 30° C (59° to 86°F). • Keep bottle tightly closed. • Active ingredients are micro-diluted in accordance with the Homeopathic Pharmacopoeia of the United States and are therefore non-toxic with no known side effects or contraindications. • Eye Floaters ® Homeopathic Sterile Eye Drops are homeopathic dilutions, for details see www.thereliefproducts.com.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Benzalkonium Chloride (preservative), Purified water, Sodium Chloride, Sodium Phosphate DiBasic, Sodium Phosphate Monobasic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCartonLabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17312-098-152025-11-17C16284748780-11e7a6dab-1666-a2ce-e063-dadaa90aadf7Natural Eyes Floaters Relief TM
17312-098-152024-07-30C16284748780-11e7a6dab-1666-a2ce-e063-dadaa90aadf7Natural Eyes Floaters Relief TM

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17312-098FLOATERS RELIEF (CHELIDONIUM MAJUS, PHYSOSTIGMA VENENOSUM SEED, EUPHRASIA STRICTA,POTASSIUM SULFATE, SODIUM CHLORIDE, PHOSPHORUS, SILICON DIOXIDE, SEPIA OFFICINALIS JUICE) LIQUID [TRP COMPANY]1Legacy NDC20220811_e5d71b42-a314-8d35-e053-2a95a90a85b4.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
17312-09817312-098-15

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
43d308bb-fa8f-9f9d-e063-6394a90ab45be5d71b42-a314-8d35-e053-2a95a90a85b42025-11-17WarningsExact identifier
spl set id: e5d71b42-a314-8d35-e053-2a95a90a85b4

Reported adverse events (FAERS/openFDA)#

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