NDC 59779-042 Eye Allergy Relief
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 59779-042?
What are the uses for Eye Allergy Relief?
Which are Eye Allergy Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D)
- NAPHAZOLINE (UNII: H231GF11BV) (Active Moiety)
- PHENIRAMINE MALEATE (UNII: NYW905655B)
- PHENIRAMINE (UNII: 134FM9ZZ6M) (Active Moiety)
Which are Eye Allergy 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)
- BORIC ACID (UNII: R57ZHV85D4)
- EDETATE SODIUM (UNII: MP1J8420LU)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- WATER (UNII: 059QF0KO0R)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Eye Allergy Relief?
- RxCUI: 1043704 - naphazoline HCl 0.02675 % / pheniramine maleate 0.315 % Ophthalmic Solution
- RxCUI: 1043704 - naphazoline hydrochloride 0.27 MG/ML / pheniramine maleate 3.15 MG/ML Ophthalmic Solution
- RxCUI: 1043704 - naphazoline HCl 0.027 % / pheniramine maleate 0.315 % Ophthalmic Solution
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[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".