NDC 55045-1194 Neomycin And Polymyxin B Sulfates And Gramicidin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55045 - Dispensing Solutions, Inc.
- 55045-1194 - Neomycin And Polymyxin B Sulfates And Gramicidin
Product Packages
NDC Code 55045-1194-2
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 55045-1194?
What are the uses for Neomycin And Polymyxin B Sulfates And Gramicidin?
Which are Neomycin And Polymyxin B Sulfates And Gramicidin UNII Codes?
The UNII codes for the active ingredients in this product are:
- NEOMYCIN SULFATE (UNII: 057Y626693)
- NEOMYCIN (UNII: I16QD7X297) (Active Moiety)
- POLYMYXIN B SULFATE (UNII: 19371312D4)
- POLYMYXIN B (UNII: J2VZ07J96K) (Active Moiety)
- GRAMICIDIN (UNII: 5IE62321P4)
- GRAMICIDIN (UNII: 5IE62321P4) (Active Moiety)
Which are Neomycin And Polymyxin B Sulfates And Gramicidin 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ALCOHOL (UNII: 3K9958V90M)
- POLOXAMER 188 (UNII: LQA7B6G8JG)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- AMMONIA (UNII: 5138Q19F1X)
What is the NDC to RxNorm Crosswalk for Neomycin And Polymyxin B Sulfates And Gramicidin?
- RxCUI: 310594 - gramicidin 0.025 MG / neomycin sulfate 1.75 MG / polymyxin B sulfate 10,000 UNT per ML Ophthalmic Solution
- RxCUI: 310594 - gramicidin 0.025 MG/ML / neomycin 1.75 MG/ML / polymyxin B 10000 UNT/ML Ophthalmic Solution
- RxCUI: 310594 - gramicidin 0.025 MG / neomycin (as neomycin sulfate) 1.75 MG / polymyxin B (as polymyxin B sulfate) 10,000 UNT per 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".