NDC 72133-121 Personal Care Cocoa Butter
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72133 - Delta Brands & Products Llc
- 72133-121 - Personal Care
Product Packages
NDC Code 72133-121-45
Package Description: 127 g in 1 TUBE
Product Details
What is NDC 72133-121?
What are the uses for Personal Care Cocoa Butter?
Which are Personal Care 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 Personal Care 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:
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- WATER (UNII: 059QF0KO0R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERIN (UNII: PDC6A3C0OX)
- MINERAL OIL (UNII: T5L8T28FGP)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- COCOA BUTTER (UNII: 512OYT1CRR)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- LAURETH-20 (UNII: 6SU0SC83AH)
- DIMETHICONE (UNII: 92RU3N3Y1O)
What is the NDC to RxNorm Crosswalk for Personal Care 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".