NDC 59985-310 Remedi Health Solutions Irritable Eye Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59985 - Chc Montana
- 59985-310 - Remedi Health Solutions
Product Packages
NDC Code 59985-310-32
Package Description: 1 BOTTLE, SPRAY in 1 BOX / 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 59985-310?
What are the uses for Remedi Health Solutions Irritable Eye Relief?
Which are Remedi Health Solutions Irritable Eye Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ALUMINUM OXIDE (UNII: LMI26O6933) (Active Moiety)
- AMYL NITRITE (UNII: 22T8Z09XAK)
- AMYL NITRITE (UNII: 22T8Z09XAK) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- ARSENIC TRIIODIDE (UNII: 3029988O2T)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- EUPHRASIA STRICTA (UNII: C9642I91WL)
- EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
- PHYSOSTIGMA VENENOSUM SEED (UNII: CJV9E9IIOA)
- PHYSOSTIGMA VENENOSUM SEED (UNII: CJV9E9IIOA) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
Which are Remedi Health Solutions Irritable Eye Relief 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)
- ALCOHOL (UNII: 3K9958V90M)
* Please review the disclaimer below.
[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".