NDC 52565-005 Hydrocortisone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 52565-005?
What are the uses for Hydrocortisone?
Which are Hydrocortisone UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCORTISONE (UNII: WI4X0X7BPJ)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
Which are 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:
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYSORBATE 40 (UNII: STI11B5A2X)
- PROPYLENE GLYCOL STEARATE (UNII: MZM1I680W0)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- SORBITAN MONOPALMITATE (UNII: 77K6Z421KU)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- TROLAMINE (UNII: 9O3K93S3TK)
- SORBIC ACID (UNII: X045WJ989B)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Hydrocortisone?
- RxCUI: 197785 - hydrocortisone 2.5 % Topical Lotion
- RxCUI: 197785 - hydrocortisone 25 MG/ML Topical Lotion
* 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".