NDC 72036-406 Harris Teeter Maximum Strength Anti-itch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72036 - Harris Teeter
- 72036-406 - Harris Teeter Maximum Strength Anti-itch
Product Packages
NDC Code 72036-406-28
Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Details
What is NDC 72036-406?
What are the uses for Harris Teeter Maximum Strength Anti-itch?
Which are Harris Teeter Maximum Strength Anti-itch UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCORTISONE (UNII: WI4X0X7BPJ)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
Which are Harris Teeter Maximum Strength Anti-itch 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)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PETROLATUM (UNII: 4T6H12BN9U)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
What is the NDC to RxNorm Crosswalk for Harris Teeter Maximum Strength Anti-itch?
- RxCUI: 203105 - hydrocortisone 1 % Topical Ointment
- RxCUI: 203105 - hydrocortisone 0.01 MG/MG Topical Ointment
* 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".