NDC 54868-3250 Neomycin, Polymyxin B Sulfates And Hydrocortisone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-3250 - Neomycin, Polymyxin B Sulfates And Hydrocortisone
Product Packages
NDC Code 54868-3250-1
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 7.5 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-3250?
What are the uses for Neomycin, Polymyxin B Sulfates And Hydrocortisone?
Which are Neomycin, Polymyxin B Sulfates And Hydrocortisone 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)
- HYDROCORTISONE (UNII: WI4X0X7BPJ)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
Which are Neomycin, Polymyxin B Sulfates And Hydrocortisone 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:
- THIMEROSAL (UNII: 2225PI3MOV)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- MINERAL OIL (UNII: T5L8T28FGP)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SULFURIC ACID (UNII: O40UQP6WCF)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Neomycin, Polymyxin B Sulfates And Hydrocortisone?
- RxCUI: 204874 - neomycin sulfate 0.35 % / polymyxin B sulfate 10,000 UNT/ML / hydrocortisone 1 % Ophthalmic Suspension
- RxCUI: 204874 - hydrocortisone 10 MG/ML / neomycin 3.5 MG/ML / polymyxin B 10000 UNT/ML Ophthalmic Suspension
- RxCUI: 204874 - hydrocortisone 1 % / neomycin (neomycin sulfate) 0.35 % / polymyxin B (polymyxin B sulfate) 10,000 UNT/ML Ophthalmic Suspension
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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".