NDC 17312-039 Eye Floaters Relief

Chelidonium Majus, Physostigma Venenosum Seed, Euphrasia Stricta,potassium Sulfate, Sodium Chloride, Phosphorus, Silicon Dioxide, Sepia Officinalis Juice

NDC Product Code 17312-039

NDC Code: 17312-039

Proprietary Name: Eye Floaters Relief What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Chelidonium Majus, Physostigma Venenosum Seed, Euphrasia Stricta,potassium Sulfate, Sodium Chloride, Phosphorus, Silicon Dioxide, Sepia Officinalis Juice What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 17312 - Trp Company
    • 17312-039 - Eye Floaters Relief

NDC 17312-039-15

Package Description: 1 BOTTLE, DROPPER in 1 PACKAGE > 10 mL in 1 BOTTLE, DROPPER

NDC Product Information

Eye Floaters Relief with NDC 17312-039 is a a human over the counter drug product labeled by Trp Company. The generic name of Eye Floaters Relief is chelidonium majus, physostigma venenosum seed, euphrasia stricta,potassium sulfate, sodium chloride, phosphorus, silicon dioxide, sepia officinalis juice. The product's dosage form is liquid and is administered via ophthalmic form.

Labeler Name: Trp Company

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Eye Floaters Relief Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • PHOSPHORUS 12 [hp_X]/mL
  • SODIUM CHLORIDE 10 [hp_X]/mL
  • SILICON DIOXIDE 12 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Ophthalmic - Administration to the external eye.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Trp Company
Labeler Code: 17312
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 05-28-2018 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Eye Floaters Relief Product Label Images

Eye Floaters Relief Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active IngredientsPurposeChelidonium HPUS 6xFloaters obstructing visionPhysostigma HPUS 12xShapes in visionEuphrasia HPUS 6xIrritationKali Sulph. HPUS 10xSquiggly lines in visionNatrium muriaticum HPUS 10xFloaters in visionPhosphorus HPUS 12xDark dots in visionSilicea HPUS 12xBlurry visionSepia HPUS 7xDust particles"HPUS" indicates the active ingredients are in the Homeopathic Pharmacopoeia of the United States.

Indications & Usage

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: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.

  • 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.

Otc - Pregnancy Or Breast Feeding

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

Do Not Use:

  • 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:

  • 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

Keep out of reach of children• In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Dosage & Administration

• 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.


  • Other information: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 Relief® Homeopathic Sterile Eye Drops are homeopathic dilutions, for details see www.thereliefproducts.com.

Inactive Ingredient

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

* Please review the disclaimer below.

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