NDC 59262-353 Allergy Eye Relief

NDC Product Code 59262-353

NDC 59262-353-12

Package Description: 20 VIAL, SINGLE-USE in 1 BOX > .4 mL in 1 VIAL, SINGLE-USE

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

NDC Product Information

Allergy Eye Relief with NDC 59262-353 is a product labeled by Similasan Corporation. The generic name of Allergy Eye Relief is . The product's dosage form is and is administered via form.

Labeler Name: Similasan Corporation

Dosage Form: -

Product Type: 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.

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)
  • SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)
  • SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)

Product Labeler Information

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

Labeler Name: Similasan Corporation
Labeler Code: 59262
Start Marketing Date: 07-02-2013 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: E 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.

Allergy 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 Ingredient

Apis 6X

Euphrasia 6X

Sabadilla 6X

Purpose

Burning, itching, stinging

Redness, swelling, watering

Watering, redness of lids

Uses:

  • According to homeopathic principles, the active ingredients in this medication temporarily relieve minor symptoms such as:itchingburningexcessive wateringredness of eyes and lids

Warnings:

  • For external use only.Initial exacerbation of symptoms may occur.
  • Use only if single-use dropper is intact.
  • To avoid contamination, do not touch the tip of the dropper to any surface. Do not reuse. Once opened, discard.
  • Contact wearers: consult a physician prior to using.

Do Not Use:

  • If solution changes color or becomes cloudy

Stop Use And Ask A Doctor If:

  • Symptoms worsen or persist for more than 72 hours
  • Changes in vision occur
  • You experience eye pain

If 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.

Directions:

  • For adults and children age 2 and over:remove a single-use droppertwist flat end with ball to removesqueeze plastic dropper to release 2-3 drops into eye and discard applicatorapply as needed throughout the day or nightuse a new dropper for every application

Other Information

Active ingredients are manufactured according to homeopathic principles.

Inactive Ingredients

Phosphate buffer, Purified water

Questions?

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

* Please review the disclaimer below.