NDC 62721-8117 Lypsyl Vanilla Plum Intense Protection
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62721 - Lornamead
- 62721-8117 - Lypsyl Vanilla Plum
Product Characteristics
Product Packages
NDC Code 62721-8117-8
Package Description: 2.83 CANISTER in 1 BLISTER PACK / 2.83 g in 1 CANISTER (62721-8117-6)
Product Details
What is NDC 62721-8117?
What are the uses for Lypsyl Vanilla Plum Intense Protection?
Which are Lypsyl Vanilla Plum Intense Protection UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Lypsyl Vanilla Plum Intense Protection 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:
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- SHEA BUTTER (UNII: K49155WL9Y)
- CERESIN (UNII: Q1LS2UJO3A)
- PARAFFIN (UNII: I9O0E3H2ZE)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
- ACAI (UNII: 46AM2VJ0AW)
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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".