NDC 54868-5251 Hydrocortisone Valerate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5251 - Hydrocortisone Valerate
Product Packages
NDC Code 54868-5251-0
Package Description: 1 TUBE in 1 CARTON / 15 g in 1 TUBE
NDC Code 54868-5251-1
Package Description: 1 TUBE in 1 CARTON / 60 g in 1 TUBE
Product Details
What is NDC 54868-5251?
What are the uses for Hydrocortisone Valerate?
Which are Hydrocortisone Valerate UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCORTISONE VALERATE (UNII: 68717P8FUZ)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
Which are Hydrocortisone Valerate 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 (UNII: 4Q93RCW27E)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-100 (UNII: 4OH5W9UM87)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PETROLATUM (UNII: 4T6H12BN9U)
- CARBOMER HOMOPOLYMER TYPE B (UNII: HHT01ZNK31)
- MINERAL OIL (UNII: T5L8T28FGP)
What is the NDC to RxNorm Crosswalk for Hydrocortisone Valerate?
- RxCUI: 1370750 - hydrocortisone valerate 0.2 % Topical Ointment
- RxCUI: 1370750 - hydrocortisone valerate 0.002 MG/MG Topical Ointment
- RxCUI: 1370754 - hydrocortisone valerate 0.2 % Topical Cream
- RxCUI: 1370754 - hydrocortisone valerate 2 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".