NDC 63868-693 Quality Choice Anti-itch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63868 - United Exchange Corp.chain Drug Marketing Association Inc.
- 63868-693 - Quality Choice Anti-itch
Product Packages
NDC Code 63868-693-28
Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Details
What is NDC 63868-693?
What are the uses for Quality Choice Anti-itch?
Which are Quality Choice 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 Quality Choice 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:
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PETROLATUM (UNII: 4T6H12BN9U)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- WHITE WAX (UNII: 7G1J5DA97F)
- ICODEXTRIN (UNII: 2NX48Z0A9G)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALUMINIUM SULFATE OCTADECAHYDRATE (UNII: TCS9L00G8F)
- CALCIUM ACETATE MONOHYDRATE (UNII: 7ZA48GIM5H)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
What is the NDC to RxNorm Crosswalk for Quality Choice Anti-itch?
- 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".