NDC 37012-063 Shopko Hydrocortisone Plus 12 Moisturizers Maximum Strength
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What is NDC 37012-063?
What are the uses for Shopko Hydrocortisone Plus 12 Moisturizers Maximum Strength?
Which are Shopko Hydrocortisone Plus 12 Moisturizers Maximum Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCORTISONE (UNII: WI4X0X7BPJ)
- HYDROCORTISONE (UNII: WI4X0X7BPJ) (Active Moiety)
Which are Shopko Hydrocortisone Plus 12 Moisturizers Maximum Strength 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:
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CORN OIL (UNII: 8470G57WFM)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MINERAL OIL (UNII: T5L8T28FGP)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PETROLATUM (UNII: 4T6H12BN9U)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Shopko Hydrocortisone Plus 12 Moisturizers Maximum Strength?
- 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
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[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".