NDC 11716-4060 Good Neighbor Pharmacy Lubricant Eye Drops
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 11716-4060?
What are the uses for Good Neighbor Pharmacy Lubricant Eye Drops?
Which are Good Neighbor Pharmacy Lubricant Eye Drops UNII Codes?
The UNII codes for the active ingredients in this product are:
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) (Active Moiety)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (Active Moiety)
Which are Good Neighbor Pharmacy Lubricant Eye Drops 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:
- BORIC ACID (UNII: R57ZHV85D4)
- CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- HYPROMELLOSE 2910 (4000 CPS) (UNII: RN3152OP35)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ZINC CHLORIDE (UNII: 86Q357L16B)
What is the NDC to RxNorm Crosswalk for Good Neighbor Pharmacy Lubricant Eye Drops?
- RxCUI: 477589 - polyethylene glycol 400, 0.4 % / propylene glycol 0.3 % Ophthalmic Solution
- RxCUI: 477589 - polyethylene glycol 400 4 MG/ML / propylene glycol 3 MG/ML Ophthalmic Solution
- RxCUI: 477589 - PEG 400 0.4 % / propylene glycol 0.3 % 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".