NDC 0536-1096 Eye Itch Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0536 - Rugby Laboratories
- 0536-1096 - Eye Itch Relief
Product Packages
NDC Code 0536-1096-40
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 5 mL in 1 BOTTLE, DROPPER
Price per Unit: $1.52526 per ML
Product Details
What is NDC 0536-1096?
What are the uses for Eye Itch Relief?
Which are Eye Itch Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- KETOTIFEN FUMARATE (UNII: HBD503WORO)
- KETOTIFEN (UNII: X49220T18G) (Active Moiety)
Which are Eye Itch Relief Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Eye Itch Relief?
- RxCUI: 311237 - ketotifen 0.025 % Ophthalmic Solution
- RxCUI: 311237 - ketotifen 0.25 MG/ML Ophthalmic Solution
- RxCUI: 311237 - ketotifen 0.025 % (as ketotifen fumarate 0.035 % ) Ophthalmic Solution
- RxCUI: 311237 - ketotifen 0.25 MG/ML (as ketotifen fumarate 0.35 MG/ML) Ophthalmic Solution
* Please review the disclaimer below.
Patient Education
Ketotifen Ophthalmic
Ophthalmic ketotifen is used to relieve the itching of allergic pinkeye. Ketotifen is in a class of medications called antihistamines. It works by blocking histamine, a substance in the body that causes allergic symptoms.
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* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".