NDC 80641-201 Vacation Lip Trips Desserts
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 80641-201?
What are the uses for Vacation Lip Trips Desserts?
Which are Vacation Lip Trips Desserts UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Vacation Lip Trips Desserts 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- C18-38 ALKYL HYDROXYSTEAROYL STEARATE (UNII: WW4FVB2PEM)
- CANOLA OIL (UNII: 331KBJ17RK)
- COCONUT OIL (UNII: Q9L0O73W7L)
- CANDELILLA WAX (UNII: WL0328HX19)
- SOYBEAN OIL (UNII: 241ATL177A)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- CASTOR OIL (UNII: D5340Y2I9G)
- ROSEMARY (UNII: IJ67X351P9)
- JOJOBA OIL (UNII: 724GKU717M)
- STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
- COCOA BUTTER (UNII: 512OYT1CRR)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
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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".