NDC 47046-170 Lucky Super Soft Cocoa Butter
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 47046 - Anicare Pharmaceuticals Pvt. Ltd.
- 47046-170 - Lucky Super Soft
Product Packages
NDC Code 47046-170-01
Package Description: 127 g in 1 TUBE
Product Details
What is NDC 47046-170?
What are the uses for Lucky Super Soft Cocoa Butter?
Which are Lucky Super Soft Cocoa Butter UNII Codes?
The UNII codes for the active ingredients in this product are:
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Lucky Super Soft Cocoa Butter 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:
- WATER (UNII: 059QF0KO0R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- GLYCERIN (UNII: PDC6A3C0OX)
- MINERAL OIL (UNII: T5L8T28FGP)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- COCOA BUTTER (UNII: 512OYT1CRR)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Lucky Super Soft Cocoa Butter?
- RxCUI: 1043075 - petrolatum 30 % Topical Cream
- RxCUI: 1043075 - petrolatum 300 MG/ML 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".