NDC 71649-3776 Xlentskin
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Product Details
What is NDC 71649-3776?
What are the uses for Xlentskin?
Which are Xlentskin UNII Codes?
The UNII codes for the active ingredients in this product are:
- LANOLIN (UNII: 7EV65EAW6H)
- LANOLIN (UNII: 7EV65EAW6H) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Xlentskin 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:
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
- PISTACIA LENTISCUS RESIN (UNII: 7446H202QW)
- MYRRH (UNII: JC71GJ1F3L)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SESAME OIL (UNII: QX10HYY4QV)
What is the NDC to RxNorm Crosswalk for Xlentskin?
- RxCUI: 1941523 - lanolin 15.5 % / petrolatum 30 % Topical Ointment
- RxCUI: 1941523 - lanolin 0.155 MG/MG / petrolatum 0.3 MG/MG Topical Ointment
- RxCUI: 1941523 - lanolin 15.5 GM per 100 GM / petrolatum 30 GM per 100 GM Topical Ointment
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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".