NDC 52862-018 Health Smart Creamy Petroleum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52862 - International Wholesale Inc Dba Home Smart Products
- 52862-018 - Health Smart Creamy Petroleum
Product Packages
NDC Code 52862-018-33
Package Description: 128 g in 1 TUBE
Product Details
What is NDC 52862-018?
What are the uses for Health Smart Creamy Petroleum?
Which are Health Smart Creamy Petroleum UNII Codes?
The UNII codes for the active ingredients in this product are:
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Health Smart Creamy Petroleum 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)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- MINERAL OIL (UNII: T5L8T28FGP)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TROLAMINE (UNII: 9O3K93S3TK)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Health Smart Creamy Petroleum?
- RxCUI: 1037285 - petrolatum 30 % Topical Gel
- RxCUI: 1037285 - petrolatum 0.3 MG/MG Topical Gel
- RxCUI: 1037285 - petrolatum 30 % Topical Jelly
* 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".