NDC 54868-1531 Cortisporin
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 54868-1531?
What are the uses for Cortisporin?
Which are Cortisporin 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 ACETATE (UNII: 3X7931PO74)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
Which are Cortisporin 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:
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- PETROLATUM (UNII: 4T6H12BN9U)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Cortisporin?
- RxCUI: 1542804 - hydrocortisone acetate 0.5 % / neomycin 0.35 % / polymyxin B 10,000 UNT/ML Topical Cream
- RxCUI: 1542804 - hydrocortisone acetate 5 MG/ML / neomycin 3.5 MG/ML / polymyxin B 10000 UNT/ML Topical Cream
- RxCUI: 1542804 - hydrocortisone acetate 0.5 % / neomycin 0.35 % (as neomycin sulfate) / polymyxin B 10,000 UNT/ML Topical Cream
- RxCUI: 1542806 - CORTISPORIN 0.5 % / 0.35 % / 10,000 UNT per GM Topical Cream
- RxCUI: 1542806 - hydrocortisone acetate 5 MG/ML / neomycin 3.5 MG/ML / polymyxin B 10000 UNT/ML Topical Cream [Cortisporin]
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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".