NDC 0363-6842 Walgreens Dual Action Lubricant Eye
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreen Company
- 0363-6842 - Walgreens Dual Action Lubricant Eye
Product Packages
NDC Code 0363-6842-15
Package Description: 2 BOTTLE, DROPPER in 1 BOX / 15 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 0363-6842?
What are the uses for Walgreens Dual Action Lubricant Eye?
Which are Walgreens Dual Action Lubricant Eye UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Walgreens Dual Action Lubricant Eye 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)
- CALCIUM CHLORATE DIHYDRATE (UNII: BBB2RG413E)
- ERYTHRITOL (UNII: RA96B954X6)
- LEVOCARNITINE (UNII: 0G389FZZ9M)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- WATER (UNII: 059QF0KO0R)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
What is the NDC to RxNorm Crosswalk for Walgreens Dual Action Lubricant Eye?
- RxCUI: 1100650 - carboxymethylcellulose sodium 0.5 % / glycerin 0.9 % Ophthalmic Solution
- RxCUI: 1100650 - carboxymethylcellulose sodium 5 MG/ML / glycerin 9 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".