NDC 73398-113 Petroleum Jelly Cocoa Butter
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73398 - Suhan Aerosol
- 73398-113 - Petroleum Jelly Cocoa Butter
Product Characteristics
Product Packages
NDC Code 73398-113-01
Package Description: 128 g in 1 TUBE
Product Details
What is NDC 73398-113?
What are the uses for Petroleum Jelly Cocoa Butter?
Which are Petroleum Jelly 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 Petroleum Jelly 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)
- MINERAL OIL (UNII: T5L8T28FGP)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETETH-20 (UNII: I835H2IHHX)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- COCOA BUTTER (UNII: 512OYT1CRR)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Petroleum Jelly 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".