NDC 54868-2143 Hydrocortisone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-2143 - Hydrocortisone
Product Packages
NDC Code 54868-2143-0
Package Description: 1 TUBE in 1 CARTON / 20 g in 1 TUBE
NDC Code 54868-2143-1
Package Description: 1 TUBE in 1 CARTON / 30 g in 1 TUBE
NDC Code 54868-2143-2
Package Description: 453.6 g in 1 JAR
Product Details
What is NDC 54868-2143?
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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SORBIC ACID (UNII: X045WJ989B)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- WHITE WAX (UNII: 7G1J5DA97F)
What is the NDC to RxNorm Crosswalk for Hydrocortisone?
- RxCUI: 310891 - hydrocortisone 2.5 % Topical Cream
- RxCUI: 310891 - hydrocortisone 25 MG/ML Topical Cream
* 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".