NDC 71486-8036 Glint Vitamin A D
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71486 - Glint Cosmetics Private Limited
- 71486-8036 - Glint
Product Packages
NDC Code 71486-8036-2
Package Description: 100 g in 1 TUBE
NDC Code 71486-8036-3
Package Description: 425 g in 1 JAR
Product Details
What is NDC 71486-8036?
What are the uses for Glint Vitamin A D?
Which are Glint Vitamin A D UNII Codes?
The UNII codes for the active ingredients in this product are:
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Glint Vitamin A D 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:
- LANOLIN (UNII: 7EV65EAW6H)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CORN OIL (UNII: 8470G57WFM)
- QUATERNIUM-15 (UNII: E40U03LEM0)
What is the NDC to RxNorm Crosswalk for Glint Vitamin A D?
- RxCUI: 1049072 - petrolatum 76 % Topical Ointment
- RxCUI: 1049072 - petrolatum 0.76 MG/MG 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".