NDC 47046-176 Lucky Supersoft Maximum Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 47046 - Anicare Pharmaceuticals Pvt. Ltd.
- 47046-176 - Lucky Supersoft
Product Packages
NDC Code 47046-176-01
Package Description: 14 g in 1 TUBE
Product Details
What is NDC 47046-176?
What are the uses for Lucky Supersoft Maximum Strength?
Which are Lucky Supersoft 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 Lucky Supersoft 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALUMINUM SULFATE (UNII: 34S289N54E)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CALCIUM ACETATE (UNII: Y882YXF34X)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ICODEXTRIN (UNII: 2NX48Z0A9G)
- GLYCERIN (UNII: PDC6A3C0OX)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Lucky Supersoft 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
* 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".