NDC 53799-378 Dry Eye Nighttime
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53799 - Similasan Ag
- 53799-378 - Dry Eye Nighttime
Product Packages
NDC Code 53799-378-11
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 53799-378?
What are the uses for Dry Eye Nighttime?
Which are Dry Eye Nighttime UNII Codes?
The UNII codes for the active ingredients in this product are:
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- EUPHRASIA STRICTA (UNII: C9642I91WL)
- EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
- MERCURIC CHLORIDE (UNII: 53GH7MZT1R)
- MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
Which are Dry Eye Nighttime 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:
- WATER (UNII: 059QF0KO0R)
- SILVER SULFATE (UNII: 8QG6HV4ZPO)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM NITRATE (UNII: 8M4L3H2ZVZ)
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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".