NDC 49035-883 Equate Day And Night Restore Tears
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49035-883?
What are the uses for Equate Day And Night Restore Tears?
Which are Equate Day And Night Restore Tears UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) (Active Moiety)
- MINERAL OIL (UNII: T5L8T28FGP)
- MINERAL OIL (UNII: T5L8T28FGP) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Equate Day And Night Restore Tears 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)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- WATER (UNII: 059QF0KO0R)
- CHLORINE DIOXIDE (UNII: 8061YMS4RM)
- POLIHEXANIDE (UNII: 322U039GMF)
- LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
What is the NDC to RxNorm Crosswalk for Equate Day And Night Restore Tears?
- RxCUI: 1188426 - carboxymethylcellulose sodium 0.5 % Ophthalmic Solution
- RxCUI: 1188426 - carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution
- RxCUI: 1188426 - carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic Solution
- RxCUI: 2046521 - {1 (15 ML) (carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution) / 1 (3500 MG) (mineral oil 0.425 MG/MG / petrolatum 0.573 MG/MG Ophthalmic Ointment) } Pack
- RxCUI: 2046521 - carboxymethylcellulose sodium 0.5 % Ophthalmic Solution (15 mL) / mineral oil 42.5 % / petrolatum 57.3 % Ophthalmic Ointment (3.5 GM) Pack
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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".