NDC 21695-529 Hydrocortisone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-529 - Hydrocortisone
Product Packages
NDC Code 21695-529-01
Package Description: 28.35 g in 1 TUBE
Product Details
What is NDC 21695-529?
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:
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- GLYCERIN (UNII: PDC6A3C0OX)
- PARAFFIN (UNII: I9O0E3H2ZE)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- LACTIC ACID (UNII: 33X04XA5AT)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Hydrocortisone?
- RxCUI: 106258 - hydrocortisone 1 % Topical Cream
- RxCUI: 106258 - hydrocortisone 10 MG/ML Topical Cream
- RxCUI: 106258 - hydrocortisone 1 % (as hydrocortisone acetate 1.2 % ) Topical Cream
- RxCUI: 106258 - hydrocortisone 1 GM per 100 GM 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".