NDC 59262-374 Dry Eye Relief

Atropa Belladonna, Euphrasia Stricta And Mercuric Chloride

NDC Product Code 59262-374

NDC Code: 59262-374

Proprietary Name: Dry Eye Relief Additional informationCallout TooltipWhat 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: Atropa Belladonna, Euphrasia Stricta And Mercuric Chloride Additional informationCallout TooltipWhat 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.


Code Structure
  • 59262 - Similasan Corporation
    • 59262-374 - Dry Eye Relief

NDC 59262-374-11

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

NDC Product Information

Dry Eye Relief with NDC 59262-374 is a a human over the counter drug product labeled by Similasan Corporation. The generic name of Dry Eye Relief is atropa belladonna, euphrasia stricta and mercuric chloride. The product's dosage form is solution/ drops and is administered via ophthalmic form.

Labeler Name: Similasan Corporation

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

Product Type: Human Otc Drug Additional informationCallout TooltipWhat 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.


Dry Eye Relief Active Ingredient(s)

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

  • ATROPA BELLADONNA 6 [hp_X]/10mL
  • EUPHRASIA STRICTA 6 [hp_X]/10mL
  • MERCURIC CHLORIDE 6 [hp_X]/10mL

Inactive Ingredient(s)

Additional informationCallout TooltipAbout 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)
  • SILVER SULFATE (UNII: 8QG6HV4ZPO)
  • SODIUM NITRATE (UNII: 8M4L3H2ZVZ)

Administration Route(s)

Additional informationCallout TooltipWhat 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

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

* Please review the disclaimer below.

Dry Eye Relief Product Label Images

Dry Eye 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

Active Ingredients

Belladonna† 6XEuphrasia officinalis (Eyebright) 6XMercurius sublimatus 15X

Purpose

Dryness, rednessrednessdryness

Uses*

According to homeopathic principles, the active ingredients in this product temporarily relieve minor symptoms such as:• dry eye• redness of eyes and lids• reflex watering secondary to dry eye

Warnings

• For external use only.• According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms).• Replace cap tightly after every use.• To avoid contamination, do not touch the tip of the bottle to any surface.• To avoid contamination use within 30 days of opening. Expiration date only refers to unopened bottle.• Contact wearers: consult a physician prior to using.

If Pregnant, Trying To Get Pregnant Or Breast Feeding,

Ask a health professional before use.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Do Not Use:

• if the solution changes color or becomes cloudy

Stop Use And Ask A Doctor If:

• symptoms worsen or persist for more than 72 hours• you experience eye pain or changes in vision

Directions

For adults and children age 2 and over:• remove tamper-evident seal from neck of bottle• twist cap off bottle• DON'T squeeze bottle, squeeze plastic tip to release 2-3 drops into eye• apply as needed• replace cap after use

Other Information

Active ingredients are manufactured according to homeopathic principles.

Inactive Ingredients

Borate buffer, Purified water, Silver sulfate (as preservative), Sodium nitrate

Questions?

Reach our representatives at 1-800-240-9780 or getinfo@similasanusa.com.www.SimilasanUSA.com

* Please review the disclaimer below.

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