NDC 68703-321 Eyeclear Pro

Calc Carb, Calc Fluor, Causticum,cineraria, Euphrasia, Naphthalinum, Nat Mur, Phos, Quassia, Silicea

NDC Product Code 68703-321

NDC Code: 68703-321

Proprietary Name: Eyeclear Pro 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: Calc Carb, Calc Fluor, Causticum,cineraria, Euphrasia, Naphthalinum, Nat Mur, Phos, Quassia, Silicea 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

  • 68703 - Silver Star Brands
    • 68703-321 - Eyeclear Pro

NDC 68703-321-02

Package Description: 59 mL in 1 BOTTLE, GLASS

NDC Product Information

Eyeclear Pro with NDC 68703-321 is a a human over the counter drug product labeled by Silver Star Brands. The generic name of Eyeclear Pro is calc carb, calc fluor, causticum,cineraria, euphrasia, naphthalinum, nat mur, phos, quassia, silicea. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Silver Star Brands

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.

Eyeclear Pro 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.

  • CAUSTICUM 10 [hp_X]/59mL
  • EUPHRASIA STRICTA 10 [hp_X]/59mL
  • NAPHTHALENE 10 [hp_X]/59mL
  • QUASSIA AMARA WOOD 10 [hp_X]/59mL
  • JACOBAEA MARITIMA 10 [hp_X]/59mL
  • SILICON DIOXIDE 10 [hp_X]/59mL
  • PHOSPHORUS 10 [hp_X]/59mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 10 [hp_X]/59mL
  • CALCIUM FLUORIDE 10 [hp_X]/59mL
  • SODIUM CHLORIDE 10 [hp_X]/59mL

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.

  • GLYCERIN (UNII: PDC6A3C0OX)
  • 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.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Silver Star Brands
Labeler Code: 68703
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: 03-04-2019 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: 12-31-2020 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.

Eyeclear Pro 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

Hpus Active Ingredients

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*

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: 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

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 Ingredients: USP purified water, vegetable glycerin.

Otc - Keep Out Of Reach Of Children

Keep this and all medication out of reach of children.

Otc - Pregnancy Or Breast Feeding

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

Otc - Purpose

Relieves symptoms of mineral buildup & eye irritation.

* Please review the disclaimer below.

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