NDC 40046-0053 Lip Conditioner Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 40046-0053?
Which are Lip Conditioner Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Lip Conditioner Spf 15 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:
- CASTOR OIL (UNII: D5340Y2I9G)
- CERESIN (UNII: Q1LS2UJO3A)
- CANDELILLA WAX (UNII: WL0328HX19)
- MYRISTYL LACTATE (UNII: 1D822OC34X)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- WHEAT GERM OIL (UNII: 14C97E680P)
- ALMOND OIL (UNII: 66YXD4DKO9)
- SHEA BUTTER (UNII: K49155WL9Y)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- ASTROCARYUM MURUMURU SEED BUTTER (UNII: 12V64UPU6R)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SACCHARIN (UNII: FST467XS7D)
- LEVOMENOL (UNII: 24WE03BX2T)
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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".