NDC 0363-1677 Walgreens Sterile Advance Relief Eye Drops
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreen Company
- 0363-1677 - Walgreens Sterile Advance Relief Eye Drops
Product Packages
NDC Code 0363-1677-15
Package Description: 1 BOTTLE, DROPPER in 1 BOX / 15 mg in 1 BOTTLE, DROPPER
Product Details
What is NDC 0363-1677?
What are the uses for Walgreens Sterile Advance Relief Eye Drops?
Which are Walgreens Sterile Advance Relief Eye Drops UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXTRAN 70 (UNII: 7SA290YK68)
- DEXTRAN 70 (UNII: 7SA290YK68) (Active Moiety)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (Active Moiety)
- POVIDONE (UNII: FZ989GH94E)
- POVIDONE (UNII: FZ989GH94E) (Active Moiety)
- TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D)
- TETRAHYDROZOLINE (UNII: S9U025Y077) (Active Moiety)
Which are Walgreens Sterile Advance Relief 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:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BORIC ACID (UNII: R57ZHV85D4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- WATER (UNII: 059QF0KO0R)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
What is the NDC to RxNorm Crosswalk for Walgreens Sterile Advance Relief Eye Drops?
- RxCUI: 996202 - dextran 70 0.1 % / polyethylene glycol 400 1 % / povidone 1 % / tetrahydrozoline HCl 0.05 % Ophthalmic Solution
- RxCUI: 996202 - dextran 70 1 MG/ML / polyethylene glycol 400 10 MG/ML / povidone 10 MG/ML / tetrahydrozoline hydrochloride 0.5 MG/ML 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".