NDC 51514-0306 Alba Very Emollient Sunscreen Lip Care Spf25
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51514 - Autumn Harp, Inc.
- 51514-0306 - Alba Very Emollient Sunscreen Lip Care Spf25
Product Characteristics
Product Packages
NDC Code 51514-0306-1
Package Description: 4.2 g in 1 CONTAINER
Product Details
What is NDC 51514-0306?
What are the uses for Alba Very Emollient Sunscreen Lip Care Spf25?
Which are Alba Very Emollient Sunscreen Lip Care Spf25 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Alba Very Emollient Sunscreen Lip Care Spf25 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:
- YELLOW WAX (UNII: 2ZA36H0S2V)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- JOJOBA OIL (UNII: 724GKU717M)
- CASTOR OIL (UNII: D5340Y2I9G)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- VANILLA (UNII: Q74T35078H)
- CANDELILLA WAX (UNII: WL0328HX19)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SHEA BUTTER (UNII: K49155WL9Y)
- COCOA BUTTER (UNII: 512OYT1CRR)
- AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- SOYBEAN OIL (UNII: 241ATL177A)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- ALLANTOIN (UNII: 344S277G0Z)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
* 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".